RSRP1, arginine and serine rich protein 1, 57035

N. diseases: 13; N. variants: 8
Disease: Hemolytic disease of fetus OR newborn due to RhD isoimmunization ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs146093871
rs146093871
Entrez Id: 6007;57035
Gene Symbol: RHD;RSRP1
RHD;RSRP1
CUI: C0158962
Disease:
Hemolytic disease of fetus OR newborn due to RhD isoimmunization 		A 0.700 SusceptibilityMutation CLINVAR Anti-D in a mother, hemizygous for the variant RHD*DNB gene, associated with hemolytic disease of the fetus and newborn. 28639307 2017