Test Code |
Test Name |
Location |
Methodology |
Disease Category |
MRP |
Days |
MGM674
|
Muscular dystrophy & congenital myopathy gene panel[Expedited TAT] |
Bangalore |
Next Generation Sequencing |
Neurology-neuromuscular |
15000 |
16 |
MGM675
|
Myotonia congenita gene panel[Expedited TAT] |
Bangalore |
Next Generation Sequencing |
Neurology-neuromuscular |
15000 |
16 |
MGM702
|
Bardet-Biedl syndrome gene panel[Expedited TAT] |
Bangalore |
Next Generation Sequencing |
Rare inherited diseases |
15000 |
16 |
MGM703
|
Congenital cataract gene panel[Expedited TAT] |
Bangalore |
Next Generation Sequencing |
Ophthalmology |
15000 |
16 |
MGM704
|
Congenital stationary night blindness gene panel[Expedited TAT] |
Bangalore |
Next Generation Sequencing |
Ophthalmology |
15000 |
16 |
MGM705
|
Leber congenital amaurosis gene panel[Expedited TAT] |
Bangalore |
Next Generation Sequencing |
Ophthalmology |
15000 |
16 |
MGM706
|
Microphthalmia and anophthalmia gene panel[Expedited TAT] |
Bangalore |
Next Generation Sequencing |
Ophthalmology |
15000 |
16 |
MGM707
|
Optic atrophy gene panel[Expedited TAT] |
Bangalore |
Next Generation Sequencing |
Ophthalmology |
15000 |
16 |
MGM715
|
Noonan syndrome gene panel[Expedited TAT] |
Bangalore |
Next Generation Sequencing |
Rare inherited diseases |
15000 |
16 |
MGM723
|
Corneal dystrophy gene panel[Expedited TAT] |
Bangalore |
Next Generation Sequencing |
Ophthalmology |
15000 |
16 |
MGM783
|
POLG gene analysis[Expedited TAT] |
Bangalore |
Next Generation Sequencing |
Rare inherited diseases |
15000 |
16 |
MGM786
|
Fukuyama Congenital Muscular Dystrophy (FKTN) gene sequencing (does not include repeat expansions)[Expedited TAT] |
Bangalore |
Next Generation Sequencing |
Neurology-neuromuscular |
15000 |
16 |
MGM585
|
Connective tissue disorder gene panel[Expedited TAT] |
Bangalore |
Next Generation Sequencing |
Connective Tissue Disorders |
25900 |
16 |
MGM586
|
Cutis-laxa gene panel[Expedited TAT] |
Bangalore |
Next Generation Sequencing |
Connective Tissue Disorders |
25900 |
16 |
MGM587
|
Ehler Danlos syndrome gene panel[Expedited TAT] |
Bangalore |
Next Generation Sequencing |
Connective Tissue Disorders |
25900 |
16 |
|
|