Test Code |
Test Name |
Location |
Methodology |
Disease Category |
MRP |
Days |
MGM244
|
Bardet-Biedl syndrome gene panel |
Bangalore |
Next Generation Sequencing |
Rare inherited diseases |
12600 |
21 |
MGM245
|
Congenital cataract gene panel |
Bangalore |
Next Generation Sequencing |
Ophthalmology |
12600 |
21 |
MGM249
|
Congenital stationary night blindness gene panel |
Bangalore |
Next Generation Sequencing |
Ophthalmology |
12600 |
21 |
MGM2500
|
DPU1086 : WHOLE MITOCHONDRIAL SEQUENCING TEST - FOR GENETIC DISORDERS (TN SCHEME) |
Bangalore |
Next Generation Sequencing |
Rare inherited diseases |
6400 |
16 |
MGM252
|
Leber congenital amaurosis gene panel |
Bangalore |
Next Generation Sequencing |
Ophthalmology |
12600 |
21 |
MGM254
|
Microphthalmia and anophthamia gene panel |
Bangalore |
Next Generation Sequencing |
Ophthalmology |
12600 |
21 |
MGM256
|
Optic atrophy gene panel |
Bangalore |
Next Generation Sequencing |
Ophthalmology |
12600 |
21 |
MGM259
|
Usher syndrome gene panel |
Bangalore |
Next Generation Sequencing |
Ophthalmology |
12600 |
21 |
MGM2634
|
Comprehensive Ophthalmic genetic Disorder Panel |
Bangalore |
Next Generation Sequencing |
Ophthalmology |
12600 |
23 |
MGM266
|
Noonan syndrome gene panel |
Bangalore |
Next Generation Sequencing |
Rare inherited diseases |
12600 |
21 |
MGM269
|
Smith-Lemli-Opitz syndrome (DHCR7) gene analysis |
Bangalore |
Next Generation Sequencing |
Rare inherited diseases |
12600 |
21 |
MGM303
|
Corneal dystrophy gene panel |
Bangalore |
Next Generation Sequencing |
Ophthalmology |
12600 |
21 |
MGM371
|
Von Hippel-Lindau syndrome (VHL) gene analysis |
Bangalore |
Next Generation Sequencing |
Oncology |
9500 |
23 |
MGM504
|
Sanger validation [1 variant] |
Bangalore |
Sanger Sequencing |
Other |
6400 |
16 |
MGM1646
|
Whole Genome Sequencing of MTB (Shotgun) with DNA extraction |
Bangalore |
Next Generation Sequencing |
Infectious Diseases |
13700 |
16 |
|
|