| Test Code |
Test Name |
Location |
Methodology |
Disease Category |
MRP |
Days |
|
MGM119
|
Krabbe disease (GALC) gene analysis |
Bangalore |
Next Generation Sequencing |
Neurology-neurodegenerative |
14000 |
21 |
|
MGM1190
|
Platelet-type bleeding disorder-8 (P2RY12) gene sequencing |
Bangalore |
Next Generation Sequencing |
Hematology |
14000 |
21 |
|
MGM1194
|
Congenital erythropoietic porphyria (UROS) gene sequencing |
Bangalore |
Next Generation Sequencing |
Rare inherited diseases |
14000 |
21 |
|
MGM1195
|
CASR gene sequencing |
Bangalore |
Next Generation Sequencing |
Rare inherited diseases |
14000 |
21 |
|
MGM1206
|
Factor X deficiency (F10) gene analysis |
Bangalore |
Next Generation Sequencing |
Hematology |
14000 |
21 |
|
MGM1207
|
VDR gene sequencing |
Bangalore |
Next Generation Sequencing |
Rare inherited diseases |
14000 |
21 |
|
MGM1208
|
Shwachman-Diamond syndrome (SBDS) gene sequencing |
Bangalore |
Next Generation Sequencing |
Hematology |
14000 |
21 |
|
MGM1213
|
Griscelli syndrome type I (MYO5A) gene sequencing |
Bangalore |
Next Generation Sequencing |
Rare inherited diseases |
14000 |
21 |
|
MGM1214
|
NR0B1 gene sequencing |
Bangalore |
Next Generation Sequencing |
Rare inherited diseases |
14000 |
21 |
|
MGM1217
|
ITGA3 gene sequencing |
Bangalore |
Next Generation Sequencing |
Rare inherited diseases |
14000 |
21 |
|
MGM1233
|
Carnitine palmitoyltransferase deficiency I (CPT1A) gene sequencing |
Bangalore |
Next Generation Sequencing |
Metabolic Disorders |
14000 |
21 |
|
MGM1234
|
AMHR2 gene sequencing |
Bangalore |
Next Generation Sequencing |
Rare inherited diseases |
14000 |
21 |
|
MGM1235
|
TRIM36 gene sequencing |
Bangalore |
Next Generation Sequencing |
Rare inherited diseases |
14000 |
21 |
|
MGM1236
|
PANK2 gene sequencing |
Bangalore |
Next Generation Sequencing |
Neurology-neurodegenerative |
14000 |
21 |
|
MGM1237
|
PKLR gene sequencing |
Bangalore |
Next Generation Sequencing |
Metabolic Disorders |
14000 |
21 |
|
|
|
|
