Chain472: Deafness, Nonsyndromic Sensorineural
This is a rare disease.
Example use A
Rare disease screening of newborns or adults thinking of having children. Could also be used as part of a comprehensive analysis of a person's genes.
Developer
Dr. Colby
Genetic info
Genes | Genetic variants |
---|---|
MYH14 | chr19:50762467,chr19:50774681,chr19:50713642,chr19:50713981 |
COCH | chr14:31346846,chr14:31348036,chr14:31348040,chr14:31348132,chr14:31358969,chr14:31346892,chr14:31348126 |
GJB3 | chr1:35250901,chr1:35250910 |
MYO6 | chr6:76566915 |
KCNQ4 | chr1:41285137,chr1:41285565,chr1:41285852 |
GJB2 | chr13:20763589,chr13:20763498,chr13:20763116 |
DIAPH1 | chr5:140903709 |
MTRNR1 | chrMT:963 |