RS387907169 SOST

Health Risk Chr 17:43758681
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What This Variant Does
"CLNSIG=5
Associated Conditions
Craniodiaphyseal dysplasia
autosomal dominant
SOST-related disorder
Craniodiaphyseal dysplasia
autosomal dominant
Craniodiaphyseal dysplasia
autosomal dominant
SOST-related disorder
Craniodiaphyseal dysplasia
autosomal dominant
Other Variants in SOST
rs387906320 rs104894644 rs104894645 rs150640883 rs201706408 rs758794256 rs377648601 rs757158654
Ask Dr. Hemsworth about this variant