| Test Code |
Test Name |
Location |
Methodology |
Disease Category |
MRP |
Days |
|
MGM1347
|
MCCC1 and MCCC2 gene sequencing |
Bangalore |
Next Generation Sequencing |
Metabolic Disorders |
21700 |
21 |
|
MGM1355
|
Imerslund-Gräsbeck syndrome (CUBN and AMN) gene sequencing |
Bangalore |
Next Generation Sequencing |
Nephrology |
21700 |
21 |
|
MGM1366
|
SLC52A1, SLC52A2, SLC52A3 gene sequencing |
Bangalore |
Next Generation Sequencing |
Metabolic Disorders |
21700 |
21 |
|
MGM1369
|
Familial erythrocytosis-1 (EPOR) gene sequencing |
Bangalore |
Next Generation Sequencing |
Hematology |
21700 |
21 |
|
MGM1378
|
Traboulsi syndrome (ASPH) gene sequencing |
Bangalore |
Next Generation Sequencing |
Rare inherited diseases |
21700 |
21 |
|
MGM1379
|
BMPR2 gene sequencing |
Bangalore |
Next Generation Sequencing |
Rare inherited diseases |
21700 |
21 |
|
MGM1381
|
Werner syndrome (RECQL2) gene sequencing |
Bangalore |
Next Generation Sequencing |
Rare inherited diseases |
21700 |
21 |
|
MGM1389
|
NR0B1, ABCD1, AIRE gene sequencing |
Bangalore |
Next Generation Sequencing |
Endocrinology |
21700 |
21 |
|
MGM1399
|
SERPING1 and F12 gene sequencing |
Bangalore |
Next Generation Sequencing |
Rare inherited diseases |
21700 |
21 |
|
MGM1400
|
Familial temporal lobe epilepsy-1 (LGI1) gene sequencing |
Bangalore |
Next Generation Sequencing |
Neurology-Epilepsy |
21700 |
21 |
|
MGM1401
|
KMT2D and KDM6A gene sequencing |
Bangalore |
Next Generation Sequencing |
Rare inherited diseases |
21700 |
21 |
|
MGM1403
|
GATA3 gene sequencing |
Bangalore |
Next Generation Sequencing |
Endocrinology |
21700 |
21 |
|
MGM1407
|
GGCX and VKORC1 gene sequencing |
Bangalore |
Next Generation Sequencing |
Rare inherited diseases |
21700 |
21 |
|
MGM1408
|
Parkes Weber syndrome (RASA1) gene sequencing |
Bangalore |
Next Generation Sequencing |
Rare inherited diseases |
21700 |
21 |
|
MGM1409
|
TCOF1 gene sequencing |
Bangalore |
Next Generation Sequencing |
Rare inherited diseases |
21700 |
21 |
|
|
|
|
