RS137853235 HGF

Health Risk Chr 7:81752250
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What This Variant Does
"[OMIM:?]
Associated Conditions
Autosomal recessive nonsyndromic hearing loss 39
Autosomal recessive nonsyndromic hearing loss 39
Other Variants in HGF
rs1788701297 rs900334407 rs148714837 rs145494248 rs141774517 rs147075806 rs145598174 rs367800414 rs140790665 rs769438908
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