RS750797779 SYNE4

Health Risk Chr 19:36006809
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What This Variant Does
"CLNSIG=4
Associated Conditions
Rare genetic deafness
Autosomal recessive nonsyndromic hearing loss 76
Rare genetic deafness
Autosomal recessive nonsyndromic hearing loss 76
Other Variants in SYNE4
rs587777072 rs774276326 rs199938988 rs200948076 rs200484521 rs771897813 rs760007740 rs200994810 rs141202530 rs758800042
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