| Test Code |
Test Name |
Location |
Methodology |
Disease Category |
MRP |
Days |
|
MGM1141
|
NKX2-1 gene sequencing |
Bangalore |
Next Generation Sequencing |
Neurology-Movement Disorders |
21700 |
21 |
|
MGM1145
|
FLT4 gene sequencing |
Bangalore |
Next Generation Sequencing |
Rare inherited diseases |
21700 |
21 |
|
MGM1146
|
Bohring-Opitz syndrome (ASXL1) gene sequencing |
Bangalore |
Next Generation Sequencing |
Rare inherited diseases |
21700 |
21 |
|
MGM1148
|
WISP3 gene sequencing |
Bangalore |
Next Generation Sequencing |
Skeletal dysplasia |
21700 |
21 |
|
MGM1170
|
PRNP gene sequencing |
Bangalore |
Next Generation Sequencing |
Rare inherited diseases |
21700 |
21 |
|
MGM118
|
Hypomyelination syndrome gene panel |
Bangalore |
Next Generation Sequencing |
Neurology-neurodegenerative |
21700 |
21 |
|
MGM1182
|
Gordon Holmes syndrome (RNF216 and OTUD4) gene sequencing |
Bangalore |
Next Generation Sequencing |
Neurology-neurodegenerative |
21700 |
21 |
|
MGM1183
|
FGFR2 gene sequencing |
Bangalore |
Next Generation Sequencing |
Rare inherited diseases |
21700 |
21 |
|
MGM1184
|
DNAAF2 and DNAAF5 gene sequencing |
Bangalore |
Next Generation Sequencing |
Rare inherited diseases |
21700 |
21 |
|
MGM1187
|
Factor VII deficiency (F7) gene sequencing |
Bangalore |
Next Generation Sequencing |
Hematology |
21700 |
21 |
|
MGM1193
|
Rubinstein-Taybi syndrome (CREBBP and EP300) gene sequencing |
Bangalore |
Next Generation Sequencing |
Rare inherited diseases |
21700 |
21 |
|
MGM1209
|
VPS13A and XK gene sequencing |
Bangalore |
Next Generation Sequencing |
Rare inherited diseases |
21700 |
21 |
|
MGM121
|
Leukodystrophy gene panel |
Bangalore |
Next Generation Sequencing |
Neurology-neurodegenerative |
21700 |
21 |
|
MGM1216
|
Trichohepatoenteric syndrome 1 (TTC37 and SKIV2L) gene sequencing |
Bangalore |
Next Generation Sequencing |
Rare inherited diseases |
21700 |
21 |
|
MGM1218
|
PHEX gene sequencing |
Bangalore |
Next Generation Sequencing |
Rare inherited diseases |
21700 |
21 |
|
|
|
|
