RS797044882 SMAD2

Health Risk Chr 18:47848537
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What This Variant Does
"CLNSIG=5
Associated Conditions
Inborn genetic diseases
Congenital heart defects
multiple types
8
with or without heterotaxy
Inborn genetic diseases
Congenital heart defects
multiple types
8
with or without heterotaxy
Other Variants in SMAD2
rs367537999 rs2144287574 rs2144300077 rs2511351266 rs745853643 rs2511326359 rs763972729 rs1305523001 rs2144378963 rs776149698
Ask Dr. Hemsworth about this variant