RS760956030 CLCN7

Health Risk Chr 16:1456172
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Associated Conditions
Autosomal dominant osteopetrosis 2
Inborn genetic diseases
Abnormality of the skeletal system
Autosomal recessive osteopetrosis 4
CLCN7-related disorder
Disorder of bone
Autosomal dominant osteopetrosis 2
Inborn genetic diseases
Abnormality of the skeletal system
Autosomal recessive osteopetrosis 4
CLCN7-related disorder
Disorder of bone
Other Variants in CLCN7
rs121434432 rs121434433 rs121434434 rs121434435 rs121434436 rs387907576 rs397515539 rs771365308 rs749315456 rs559965660
Ask Dr. Hemsworth about this variant