Test Code |
Test Name |
Location |
Methodology |
Disease Category |
MRP |
Days |
MGM1238
|
SLC11A2 gene sequencing |
Bangalore |
Next Generation Sequencing |
Hematology |
14000 |
21 |
MGM124
|
Ataxia-telangiectasia (ATM) gene analysis |
Bangalore |
Next Generation Sequencing |
Neurology-Movement Disorders |
14000 |
21 |
MGM1244
|
PLP1 gene sequencing |
Bangalore |
Next Generation Sequencing |
Neurology |
14000 |
21 |
MGM1245
|
SERPINC1 gene sequencing |
Bangalore |
Next Generation Sequencing |
Hematology |
14000 |
21 |
MGM1246
|
Keutel syndrome (MGP) gene sequencing |
Bangalore |
Next Generation Sequencing |
Rare inherited diseases |
14000 |
21 |
MGM1247
|
SLC4A1 gene sequencing |
Bangalore |
Next Generation Sequencing |
Rare inherited diseases |
14000 |
21 |
MGM1252
|
Fructose-1,6-bisphosphatase deficiency (FBP1) gene sequencing |
Bangalore |
Next Generation Sequencing |
Metabolic Disorders |
14000 |
21 |
MGM1253
|
Argininosuccinic aciduria (ASL) gene sequencing |
Bangalore |
Next Generation Sequencing |
Metabolic Disorders |
14000 |
21 |
MGM1262
|
HPRT1 gene sequencing |
Bangalore |
Next Generation Sequencing |
Rare inherited diseases |
14000 |
21 |
MGM1265
|
Erythropoietic protoporphyria-1 (FECH) gene sequencing |
Bangalore |
Next Generation Sequencing |
Dermatology |
14000 |
21 |
MGM1269
|
MYH3 gene sequencing |
Bangalore |
Next Generation Sequencing |
Neurology-neuromuscular |
14000 |
21 |
MGM1281
|
Neurodegeneration due to cerebral folate transport deficiency (FOLR1) gene sequencing |
Bangalore |
Next Generation Sequencing |
Neurology-neurodegenerative |
14000 |
21 |
MGM1282
|
Borjeson-Forssman-Lehmann syndrome (PHF6) gene sequencing |
Bangalore |
Next Generation Sequencing |
Rare inherited diseases |
14000 |
21 |
MGM1285
|
CYP11B1 gene sequencing |
Bangalore |
Next Generation Sequencing |
Endocrinology |
14000 |
21 |
MGM1286
|
CHM gene sequencing |
Bangalore |
Next Generation Sequencing |
Ophthalmology |
14000 |
21 |
|
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