RS104894413 GJB2

Health Risk Chr 13:20189451
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What This Variant Does
"[OMIM:?]
Associated Conditions
Autosomal dominant nonsyndromic hearing loss 3A
Inborn genetic diseases
Autosomal recessive nonsyndromic hearing loss 1A
8 conditions
Inborn genetic diseases
GJB2-related disorder
7 conditions
Autosomal dominant nonsyndromic hearing loss 3A
Inborn genetic diseases
Autosomal recessive nonsyndromic hearing loss 1A
8 conditions
Inborn genetic diseases
GJB2-related disorder
7 conditions
Other Variants in GJB2
rs35887622 rs80338944 rs104894396 rs104894397 rs80338939 rs104894398 rs80338947 rs80338950 rs80338948 rs80338942
Ask Dr. Hemsworth about this variant