RS201810925 CLCN7

Health Risk Chr 16:1447402
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Associated Conditions
Autosomal recessive osteopetrosis 4
Autosomal dominant osteopetrosis 2
Hypopigmentation
organomegaly
and delayed myelination and development
Autosomal recessive osteopetrosis 4
Autosomal dominant osteopetrosis 2
Hypopigmentation
organomegaly
and delayed myelination and development
Other Variants in CLCN7
rs121434432 rs121434433 rs121434434 rs121434435 rs121434436 rs387907576 rs397515539 rs771365308 rs749315456 rs559965660
Ask Dr. Hemsworth about this variant