RS267607042 SETBP1

Health Risk Chr 18:44951942
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What This Variant Does
"CLNSIG=5
Associated Conditions
Schinzel-Giedion syndrome
Intellectual disability
autosomal dominant 29
SETBP1-related disorder
Schinzel-Giedion syndrome
Schinzel-Giedion syndrome
Intellectual disability
autosomal dominant 29
SETBP1-related disorder
Schinzel-Giedion syndrome
Other Variants in SETBP1
rs267607038 rs267607041 rs267607039 rs267607040 rs606231269 rs672601342 rs606231270 rs606231271 rs606231272 rs606231273
Ask Dr. Hemsworth about this variant