RS376104748 STRC
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What This Variant Does
"CLNSIG=5
Associated Conditions
Rare genetic deafness
Autosomal dominant nonsyndromic hearing loss 16
Autosomal recessive nonsyndromic hearing loss 16
Nonsyndromic genetic hearing loss
Deafness-infertility syndrome
Spermatogenic failure 7
Autosomal recessive nonsyndromic hearing loss 16
Rare genetic deafness
Autosomal dominant nonsyndromic hearing loss 16
Autosomal recessive nonsyndromic hearing loss 16
Nonsyndromic genetic hearing loss
Deafness-infertility syndrome
Spermatogenic failure 7
Autosomal recessive nonsyndromic hearing loss 16
Other Variants in STRC