RS397515539 CLCN7

Health Risk Chr 16:1459139
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Autosomal dominant osteopetrosis 2
CLCN7-related disorder
Autosomal dominant osteopetrosis 2
CLCN7-related disorder
Other Variants in CLCN7
rs121434432 rs121434433 rs121434434 rs121434435 rs121434436 rs387907576 rs771365308 rs749315456 rs559965660 rs531105528
Ask Dr. Hemsworth about this variant