RS137853014 ATP2C1

Health Risk Chr 3:130975387
Upload your DNA to see your genotype for this variant.
What This Variant Does
"[OMIM:?]
Associated Conditions
Familial benign pemphigus
Familial benign pemphigus
Other Variants in ATP2C1
rs1559971447 rs137853012 rs137853013 rs1559982055 rs1560033613 rs137853015 rs748204512 rs1057518594 rs1057517706 rs1057520634
Ask Dr. Hemsworth about this variant