RS778175819 SMARCA4

Health Risk Chr 19:11021846
Upload your DNA to see your genotype for this variant.
Associated Conditions
SMARCA4-related BAFopathy
Intellectual disability
autosomal dominant 16
Medulloblastoma WNT activated
SMARCA4-related BAFopathy
Intellectual disability
autosomal dominant 16
Medulloblastoma WNT activated
Other Variants in SMARCA4
rs267607070 rs876657378 rs281875226 rs281875227 rs281875228 rs281875229 rs281875230 rs587779750 rs145867502 rs587778680
Ask Dr. Hemsworth about this variant