RS1064795322 ATP2B2

Health Risk Chr 3:10375477
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What This Variant Does
"CLNSIG=4
Associated Conditions
ATP2B2-related disorder
Hearing loss
autosomal dominant 82
ATP2B2-related disorder
Hearing loss
autosomal dominant 82
Other Variants in ATP2B2
rs1057520233 rs777396418 rs1553564078 rs1553652886 rs1575005369 rs1575009907 rs2061464108 rs1487836380 rs2125357775 rs2125368879
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