Gene panels & single-gene tests in Jammu
Focused gene tests when a specific inherited condition is suspected. 124 tests available through Jammu Genetics Hub in Jammu — open any test to see what it is for, who it is advised for, its sample type and partner-lab price.
- Congenital Adrenal Hyperplasia (CAH) Gene Analysis₹2,999
- Cystic Fibrosis (CFTR) Gene Testing₹3,999
- Fragile X Syndrome Testing₹3,999
- Spinal Muscular Atrophy (SMA) Testing₹2,799
- Achondroplasia (FGFR3) Mutations Analysis By NGS-Individual₹6,000
- Albinism Gene Panel₹22,000
- ASPA Gene del/dup By MLPA₹12,000
- Ataxia-Telangiectasia (ATM) Deletion Duplication And Gene Analysis₹25,000
- ATN1 gene CAG₹15,000
- ATP7B MLPA₹12,000
- Autism Spectrum Disorders Panel₹42,000
- C-KIT Gene NGS Sequencing₹12,000
- CFTR Gene MLPA₹12,000
- CFTR Gene Sequencing₹22,000
- Cornelia De Lange Panel₹22,000
- CYP21A2 Gene Sequencing - PND₹22,000
- CYP21A2 Gene Sequencing-Individual₹20,000
- Cystic Fibrosis Delta F508 Muation₹5,000
- Cystic Fibrosis DeltaF508 Mutation Analysis-PND₹5,000
- Deletion/Duplication Analysis Of CYP21A2 Gene-Individual₹10,000
- Deletion/Duplication Analysis Of CYP21A2 Gene-PND₹15,000
- Deletion/Duplication Analysis Of F8 Gene₹12,000
- Deletion/Duplication Analysis Of F9 Gene (Hemophilia B)₹12,000
- Deletion/Duplication Analysis of IKBKG Gene-Individual₹10,000
- Deletion/Duplication Analysis Of MECP2gene( Rett Syndrome)-Individual₹10,000
- Deletion/Duplication Analysis Of OTC Gene-Individual₹9,000
- Deletion/Duplication Analysis Of PCCA gene-individual₹12,000
- Deletion/Duplication Analysis Of RB1 Gene-PND₹10,000
- DMD - Del/Dup-MLPA + Muscular Dystrophy Panel₹25,000
- DMD 26 Exons Deletion Prenatal Diagnosis₹10,500
- Duchenne Muscular Dystrophy for MLPA₹14,000
- Dystrophin Gene Sequencing - DMD₹22,000
- Early-Onset Juvenile Parkinsonism Gene Panel₹22,000
- Epilepsy Panel₹22,000
- Factor V Leiden Mutant Detection (G1691A Mutation)₹6,200
- Factor V Leiden Mutation₹6,000
- Familial Testing₹35,000
- FGFR3 Common Mutations Study- Individual₹7,500
- FGFR3 gene sequencing₹22,000
- Fragile X Screening -PND₹35,000
- Fragile X Screening for Males₹7,000
- Fragile-X for Females₹10,000
- Fragile-X PCR Screening₹10,000
- Fragile-X Syndrome(Mehylation Test- Confirmatory)-Individual₹20,000
- Friedreich Ataxia GAA Repeat₹8,500
- G6PD Gene Sequencing₹15,000
- Hemophilia A - F8 gene sequencing₹20,000
- Hemophilia A - Inversion 1/22₹10,000
- Hereditary Multiple Exostoses-Individual₹22,000
- Hereditary Panel With Reflex to MLPA₹80,000
- HLA DQ- Alpha & Beta- Couple₹30,000
- HLA DQ- Alpha & Beta- Individual₹12,000
- HLA Typing (HLA-A, B, C, DRB1 & DQB1)-High Resolution₹15,000
- HLA Typing (HLA-A, B, DRB1)- Low Resolution₹13,000
- Ichthyosis Gene Panel₹22,000
- Incontinentia Pigmenti Nemo Gene Common Deletions₹8,000
- LAMA-2 Gene-MLPA₹12,000
- Lisscencephaly Panel by MLPA₹10,000
- Maturity-Onset Diabetes Of The Young- Individual₹22,000
- Methylation PCR for SNRPN Gene₹12,000
- Mitochondrial gene MLPA₹15,000
- Mitochondrial Gene Panel(Individual)₹18,000
- Molecular diagnosis for Huntingtons₹8,500
- Molecular diagnosis for Prader Willi₹12,000
- Molecular Diagnosis for Triplet Repeat Disorders₹12,000
- Molecular diagnosis of single gene by MLPA₹15,000
- MS MLPA for Russel Silver-Methylation H19 and UP₹12,000
- MS-MLPA for Beckwith Wideman Syndrome- Individual₹12,000
- MTHFR Mutation (C677T,A1298C )₹7,500
- MTHFR mutation analysis₹6,000
- Muscular Dystrophy&Congenital Myopathies Panel₹22,000
- Myotonic Dystrophy (Triplet Repeat Analysis)-Individual₹6,000
- Myotonic Dystrophy Type I₹12,000
- Myotonic Dystrophy Type II (Triplet Repeat Analysis)₹12,000
- Nephrology Panel₹22,000
- Neurofibromatosis Gene Panel₹25,000
- Neurofibromatosis Type 2 (NF2) Deletion/Duplication Analysis₹10,000
- Neuronal Migration Panel₹22,000
- NF1 Deletion/Duplication Analysis₹10,000
- Noonan Syndrome Panel₹22,000
- PAFAHIBI Gene By MLPA (Individual)₹12,000
- PLP1 Gene MLPA₹12,000
- PMP22 Deletion/Duplication By MLPA₹10,000
- Polycystic Kidney Disease Gene Panel Individual₹22,000
- Prenatal diagnosis for DMD (MLPA)₹15,000
- Prenatal Diagnosis For Single Gene MLPA₹35,000
- Prenatal Diagnosis for Triplet Repeat Disorders₹15,000
- Prenatal Diagnosis Of Bechwith Weidman Syndrome₹17,500
- Prenatal Diagnosis of Beckwith Wiedemann Methylation/ Russell Silver Methylation MS MLPA₹35,000
- Prenatal Diagnosis of Fragile-X Syndrome₹13,000
- Prenatal Diagnosis of Prader Willi Syndrome/ Angelman Syndrome MS MLPA₹35,000
- Prothrombin G20210A (Factor II) Mutation Detection₹5,830
- Prothrombin Gene Comman Mutation₹5,000
- Prothrombin Gene Polymorphism G20210A- Individual₹6,000
- RB1 Gene Sequencing With Deletion/ Duplication Anlysis-MLPA₹22,000
- Retinal Degeneration Panel₹22,000
- Rh-Genotyping₹22,000
- RVVT (Russell Viper Venom Time)₹1,350
- SCID-DCLRELIC MLPA₹12,000
- Single Variant Analysis- 3 Variant₹25,000
- Single Variant Analysis- Prenatal +Couple(1 Variant)₹25,000
- Single Variant Analysis-Couple₹25,000
- Single Variant Analysis-Couple (1 Variant)₹12,000
- Single Variant Analysis-Individual(1)₹6,000
- Single Variant Analysis-Individual(2)₹12,000
- Single Variant Analysis-PND(1 Variant)₹12,500
- Single Variant Analysis-PND(2)₹20,000
- Single Variant Analysis-Prenatal +Couple(2 Variants)₹40,000
- Skeletal Dysplasia Panel - Individual₹22,000
- Skeletal Dysplasia Panel-PND₹22,000
- SMA MLPA-Individual₹12,000
- SMN1 Gene Sequencing - Individual₹20,000
- Spinal Muscular Atrophy-PND₹15,000
- Spinocerebellar Ataxia (SCA 12) Repeat Expansion Analysis-Individual₹15,000
- Spinocerebellar Ataxia (SCA 2) Repeat Expansion Analysis-Individual₹4,000
- Spinocerebellar ataxia (SCA 3) repeat expansion analysis - Individual₹12,000
- Spinocerebellar Ataxia Repeat Expansion Analysis₹18,000
- Thrombophilia mutation profile₹14,000
- TSC1 Deletion/Duplication Analysis₹12,000
- TSC2 Deletion/Duplication Analysis₹12,000
- UGT1A1 gene polymorphism (Nucleotide TA repeat)₹12,000
- UGT1A1 Promoter Polymorphism -Individual₹8,500
- VHL Gene Deletion/Duplication MLPA (Individual)₹12,000
- Wilson Disease (ATP7B) Gene Analysis₹25,000
Not sure which test you need? Talk to a geneticist.
Jammu Genetics Hub helps patients in Jammu connect with BGCI-certified geneticists who explain your options, choose the right test, and walk you through your results — so you understand every report and what to do next.