RS398123036 LARS2

Health Risk Chr 3:45516118
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What This Variant Does
"CLNSIG=5
Associated Conditions
Perrault syndrome
Perrault syndrome 4
Nonsyndromic genetic hearing loss
Perrault syndrome
Perrault syndrome 4
Nonsyndromic genetic hearing loss
Other Variants in LARS2
rs199589947 rs398123037 rs786205560 rs864309642 rs864309643 rs116826217 rs199693918 rs879255606 rs879255408 rs35347543
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