Hearing Impairment
Other
255 variants
20 genes
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Associated Genes (20)
GJB2
COL11A2
ACTG1
COL4A5
MYO7A
SLC26A4
PDZD7
MYO6
WFS1
CDH23
MITF
TMIE
TYR
BSND
CLRN1
CLDN14
TMPRSS3
GJB3
COCH
USH2A
Associated Variants (255)
RSID
Gene
Risk Allele
Odds Ratio
Evidence
RS457717
—
T
—
exploratory
RS10499138
—
A
—
exploratory
RS72474224
GJB2
—
—
strong
RS104894408
GJB2
—
—
strong
RS28931593
GJB2
—
—
strong
RS80338940
GJB2
—
—
strong
RS104894409
GJB2
—
—
strong
RS121912952
COL11A2
—
—
strong
RS267606631
ACTG1
—
—
strong
RS1801002
GJB2
—
—
strong
RS80338949
GJB2
—
—
strong
RS281874743
COL4A5
—
—
strong
RS111033229
MYO7A
—
—
strong
RS200641606
MYO7A
—
—
strong
RS397516324
MYO7A
—
—
strong
RS111033309
SLC26A4
—
—
strong
RS111033310
SLC26A4
—
—
strong
RS397516636
PDZD7
—
—
strong
RS111033299
GJB2
—
—
strong
RS111033253
GJB2
—
—
strong
RS111033295
GJB2
—
—
strong
RS111033294
GJB2
—
—
strong
RS202214380
MYO6
—
—
strong
RS142668478
WFS1
—
—
strong
RS397517344
CDH23
—
—
strong
RS104893746
MITF
—
—
strong
RS28942097
TMIE
—
—
strong
RS104894313
TYR
—
—
strong
RS121908145
BSND
—
—
strong
RS121908140
CLRN1
—
—
strong
RS111033308
SLC26A4
—
—
strong
RS80338848
SLC26A4
—
—
strong
RS111033303
SLC26A4
—
—
strong
RS111033199
SLC26A4
—
—
strong
RS74315437
CLDN14
—
—
strong
RS137852999
TMPRSS3
—
—
strong
RS786200895
GJB3
—
—
strong
RS28938175
COCH
—
—
strong
RS111033364
USH2A
—
—
strong
RS35887622
GJB2
—
—
strong
RS104894396
GJB2
—
—
strong
RS104894397
GJB2
—
—
strong
RS80338939
GJB2
—
—
strong
RS104894398
GJB2
—
—
strong
RS80338947
GJB2
—
—
strong
RS80338950
GJB2
—
—
strong
RS80338948
GJB2
—
—
strong
RS80338942
GJB2
—
—
strong
RS80338943
GJB2
—
—
strong
RS104894407
GJB2
—
—
strong
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