RS765741202 CIB2

Health Risk Chr 15:78109272
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Associated Conditions
Rare genetic deafness
Autosomal recessive nonsyndromic hearing loss 48
Usher syndrome type 1J
Rare genetic deafness
Autosomal recessive nonsyndromic hearing loss 48
Usher syndrome type 1J
Other Variants in CIB2
rs2141925983 rs374836619 rs1567049981 rs1054728914 rs762127980 rs752523704 rs1363188459 rs758251566 rs1567047642 rs780168150
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