Test Code |
Test Name |
Location |
Methodology |
Disease Category |
MRP |
Days |
MGM101
|
Urea cycle defects gene panel |
Bangalore |
Next Generation Sequencing |
Metabolic Disorders |
21700 |
21 |
MGM1020
|
Newborn screening gene panel |
Bangalore |
Next Generation Sequencing |
Rare inherited diseases |
21700 |
21 |
MGM1025
|
Myelin-oligodendrocyte glycoprotein (MOG) gene sequencing |
Bangalore |
Next Generation Sequencing |
Rare inherited diseases |
21700 |
21 |
MGM1029
|
PRSS56 and MFRP gene analysis |
Bangalore |
Next Generation Sequencing |
Ophthalmology |
21700 |
21 |
MGM103
|
Alport syndrome gene panel |
Bangalore |
Next Generation Sequencing |
Nephrology |
21700 |
21 |
MGM1031
|
Holt-Oram syndrome (TBX5) gene sequencing |
Bangalore |
Next Generation Sequencing |
Skeletal dysplasia |
21700 |
21 |
MGM1037
|
Saethre-Chotzen syndrome (TWIST1 and FGFR2) gene sequencing |
Bangalore |
Next Generation Sequencing |
Rare inherited diseases |
21700 |
21 |
MGM1038
|
SHOX gene sequencing |
Bangalore |
Next Generation Sequencing |
Skeletal dysplasia |
21700 |
21 |
MGM104
|
Bartter syndrome gene panel |
Bangalore |
Next Generation Sequencing |
Nephrology |
21700 |
21 |
MGM1040
|
TIA1 and DES genes sequencing |
Bangalore |
Next Generation Sequencing |
Neurology-neuromuscular |
21700 |
21 |
MGM105
|
Meckel Gruber syndrome gene panel |
Bangalore |
Next Generation Sequencing |
Nephrology |
21700 |
21 |
MGM1056
|
Combo - NeuroMit Whole mitochondrial genome sequencing & Neurology gene panel |
Bangalore |
Next Generation Sequencing |
Other |
21700 |
21 |
MGM106
|
Polycystic kidney disease gene panel |
Bangalore |
Next Generation Sequencing |
Nephrology |
21700 |
21 |
MGM1061
|
CYB5R3 and CYB5A gene sequencing |
Bangalore |
Next Generation Sequencing |
Hematology |
21700 |
21 |
MGM1065
|
Glanzmann thrombasthenia (ITGA2B and ITGB3) gene sequencing |
Bangalore |
Next Generation Sequencing |
Hematology |
21700 |
21 |
|
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