Test Code |
Test Name |
Location |
Methodology |
Disease Category |
MRP |
Days |
MGM1036
|
SETX gene sequencing |
Bangalore |
Next Generation Sequencing |
Neurology-Movement Disorders |
14000 |
21 |
MGM1039
|
MFSD8 gene sequencing |
Bangalore |
Next Generation Sequencing |
Neurology-neurodegenerative |
14000 |
21 |
MGM1041
|
SACS gene sequencing |
Bangalore |
Next Generation Sequencing |
Neurology-Movement Disorders |
14000 |
21 |
MGM1042
|
SLC25A15 gene sequencing |
Bangalore |
Next Generation Sequencing |
Metabolic Disorders |
14000 |
21 |
MGM1043
|
KRT5 gene sequencing |
Bangalore |
Next Generation Sequencing |
Dermatology |
14000 |
21 |
MGM1049
|
ALPL gene sequencing |
Bangalore |
Next Generation Sequencing |
Rare inherited diseases |
14000 |
21 |
MGM1051
|
CFH gene sequencing |
Bangalore |
Next Generation Sequencing |
Nephrology |
14000 |
21 |
MGM1064
|
ADGRG1 gene sequencing |
Bangalore |
Next Generation Sequencing |
Neurology |
14000 |
21 |
MGM1072
|
RPGR gene sequencing |
Bangalore |
Next Generation Sequencing |
Ophthalmology |
14000 |
21 |
MGM110
|
Dravet syndrome (SCN1A) gene analysis |
Bangalore |
Next Generation Sequencing |
Neurology-Epilepsy |
14000 |
21 |
MGM1119
|
IGHMBP2 gene sequencing |
Bangalore |
Next Generation Sequencing |
Neurology-neuromuscular |
14000 |
21 |
MGM1142
|
Vitamin D-dependent rickets type 1A (CYP27B1) gene sequencing |
Bangalore |
Next Generation Sequencing |
Skeletal dysplasia |
14000 |
21 |
MGM1143
|
TULP1 gene sequencing |
Bangalore |
Next Generation Sequencing |
Ophthalmology |
14000 |
21 |
MGM1147
|
MTTP gene sequencing |
Bangalore |
Next Generation Sequencing |
Metabolic Disorders |
14000 |
21 |
MGM1149
|
SLC19A3 gene sequencing |
Bangalore |
Next Generation Sequencing |
Metabolic Disorders |
14000 |
21 |
|
|