RS137853012 ATP2C1

Health Risk Chr 3:130963981
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What This Variant Does
"[OMIM:?]
Associated Conditions
Familial benign pemphigus
Familial benign pemphigus
Other Variants in ATP2C1
rs1559971447 rs137853013 rs1559982055 rs137853014 rs1560033613 rs137853015 rs748204512 rs1057518594 rs1057517706 rs1057520634
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