RS797044953 SETD5

Health Risk Chr 3:9447684
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What This Variant Does
"CLNSIG=5
Associated Conditions
Inborn genetic diseases
Inborn genetic diseases
Other Variants in SETD5
rs587777325 rs587777326 rs587777327 rs587777328 rs587777329 rs864321657 rs1553618323 rs780263494 rs375122657 rs376767548
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