RS869312964 SMARCA4

Health Risk Chr 19:11013022
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What This Variant Does
"CLNSIG=5
Associated Conditions
Inborn genetic diseases
Inborn genetic diseases
Other Variants in SMARCA4
rs267607070 rs876657378 rs281875226 rs281875227 rs281875228 rs281875229 rs281875230 rs587779750 rs145867502 rs587778680
Ask Dr. Hemsworth about this variant