RS766705070 MAP3K7

Health Risk Chr 6:90571758
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Associated Conditions
Inborn genetic diseases
Inborn genetic diseases
Other Variants in MAP3K7
rs886039230 rs886039231 rs886039232 rs886039233 rs886039234 rs886039235 rs886039236 rs886039237 rs1057517758 rs1064795771
Ask Dr. Hemsworth about this variant