RS786204837 WNT5A

Health Risk Chr 3:55479499
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What This Variant Does
"CLNSIG=5
Associated Conditions
Autosomal dominant Robinow syndrome 1
Autosomal dominant Robinow syndrome 1
Other Variants in WNT5A
rs554762368 rs2106946273 rs2051221341 rs1231823028 rs370383438 rs375233428 rs369701725 rs761851847 rs755916316 rs946840827
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