Autosomal Dominant Nonsyndromic Hearing Loss 6

Other 230 variants 1 gene

Upload your DNA to see your personal risk score for Autosomal Dominant Nonsyndromic Hearing Loss 6.

Associated Genes (1)
Associated Variants (230)
RSID Gene Risk Allele Odds Ratio Evidence
RS146418094 WFS1 exploratory
RS757027394 WFS1 exploratory
RS71524377 WFS1 exploratory
RS776685250 WFS1 exploratory
RS200058166 WFS1 exploratory
RS140667597 WFS1 exploratory
RS876658119 WFS1 exploratory
RS771391168 WFS1 exploratory
RS564413149 WFS1 exploratory
RS727504730 WFS1 exploratory
RS755328574 WFS1 exploratory
RS727503747 WFS1 exploratory
RS756667462 WFS1 exploratory
RS760938537 WFS1 exploratory
RS756869880 WFS1 exploratory
RS1560421124 WFS1 exploratory
RS760226129 WFS1 exploratory
RS914996283 WFS1 exploratory
RS140773453 WFS1 exploratory
RS775216682 WFS1 exploratory
RS751270928 WFS1 exploratory
RS779199009 WFS1 exploratory
RS756252214 WFS1 exploratory
RS1730968028 WFS1 exploratory
RS1553878946 WFS1 exploratory
RS150771247 WFS1 strong
RS748353498 WFS1 strong
RS35031397 WFS1 strong
RS104893883 WFS1 strong
RS28937894 WFS1 strong
RS104893882 WFS1 strong
RS74315205 WFS1 strong
RS387906930 WFS1 strong
RS1801206 WFS1 strong
RS1801208 WFS1 strong
RS114152068 WFS1 strong
RS142668478 WFS1 strong
RS141328044 WFS1 strong
RS35932623 WFS1 strong
RS199946797 WFS1 strong
RS146132083 WFS1 strong
RS71539668 WFS1 strong
RS149865710 WFS1 strong
RS145677667 WFS1 strong
RS727504666 WFS1 strong
RS71524353 WFS1 strong
RS140125843 WFS1 strong
RS367547063 WFS1 strong
RS71537685 WFS1 strong
RS28937892 WFS1 strong
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