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

GenesGenetic variants
MYH14chr19:50762467,chr19:50774681,chr19:50713642,chr19:50713981
COCHchr14:31346846,chr14:31348036,chr14:31348040,chr14:31348132,chr14:31358969,chr14:31346892,chr14:31348126
GJB3chr1:35250901,chr1:35250910
MYO6chr6:76566915
KCNQ4chr1:41285137,chr1:41285565,chr1:41285852
GJB2chr13:20763589,chr13:20763498,chr13:20763116
DIAPH1 chr5:140903709
MTRNR1chrMT:963

Qualitative

Type

text

Possible responses

Carrier, Possibly Affected, Not Detected, insufficient data, error