RS587777021 GNA11

Health Risk Chr 19:3110190
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What This Variant Does
"CLNSIG=5
Associated Conditions
Autosomal dominant hypocalcemia 2
Familial hypocalciuric hypercalcemia 2
Autosomal dominant hypocalcemia 2
Familial hypocalciuric hypercalcemia 2
Other Variants in GNA11
rs1335558363 rs2145325982 rs2512096499 rs2145325959 rs373562448 rs2145326448 rs758392443 rs770720811 rs535105766 rs2145329230
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