RS755292491 NALCN

Health Risk Chr 13:101055387
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Associated Conditions
Inborn genetic diseases
Inborn genetic diseases
Other Variants in NALCN
rs587777038 rs145910377 rs869025188 rs587777068 rs786203984 rs786203985 rs786203986 rs786203987 rs786203988 rs786201003
Ask Dr. Hemsworth about this variant