RS121909283 NODAL

Health Risk Chr 10:70435399
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What This Variant Does
"[OMIM:?]
Associated Conditions
Heterotaxy
visceral
5
autosomal
Inborn genetic diseases
Wolff-Parkinson-White pattern
Visceral heterotaxy
NODAL-related disorder
Heterotaxy
visceral
5
autosomal
Inborn genetic diseases
Wolff-Parkinson-White pattern
Visceral heterotaxy
Other Variants in NODAL
rs143903715 rs2493085626 rs2493087333 rs2493096439 rs2493095831 rs2132214841 rs200445211 rs1589152355 rs781366461 rs749265748
Ask Dr. Hemsworth about this variant