RS281875227 SMARCA4

Health Risk Chr 19:11021761
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Intellectual disability
autosomal dominant 16
Inborn genetic diseases
Intellectual disability
autosomal dominant 16
Inborn genetic diseases
Other Variants in SMARCA4
rs267607070 rs876657378 rs281875226 rs281875228 rs281875229 rs281875230 rs587779750 rs145867502 rs587778680 rs587778681
Ask Dr. Hemsworth about this variant