RS797044895 GNAS

Health Risk Chr 20:58895635
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What This Variant Does
"CLNSIG=4
Associated Conditions
Inborn genetic diseases
Inborn genetic diseases
Other Variants in GNAS
rs137854530 rs1601164378 rs1601163749 rs137854531 rs137854532 rs11554273 rs121913495 rs121913494 rs137854533 rs587776829
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