RS193922649 LAMP2

Health Risk Chr X:120449063
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=4
Associated Conditions
Primary familial hypertrophic cardiomyopathy
Danon disease
Primary familial hypertrophic cardiomyopathy
Danon disease
Other Variants in LAMP2
rs137852527 rs1352584474 rs2520860264 rs1251075016 rs1183994410 rs1327363415 rs1436181133 rs104894857 rs104894858 rs200297370
Ask Dr. Hemsworth about this variant