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rs1800582

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1800582(A;A)
Make rs1800582(A;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position144119686
GeneGYPA, GYPB
is asnp
is mentioned by
dbSNPrs1800582
ebirs1800582
HLIrs1800582
Exacrs1800582
Varsomers1800582
Maprs1800582
PheGenIrs1800582
hapmaprs1800582
1000 genomesrs1800582
hgdprs1800582
ensemblrs1800582
gopubmedrs1800582
geneviewrs1800582
scholarrs1800582
googlers1800582
pharmgkbrs1800582
gwascentralrs1800582
openSNPrs1800582
23andMers1800582
23andMe allrs1800582
SNP Nexus

SNPshotrs1800582
SNPdbers1800582
MSV3drs1800582
GWAS Ctlgrs1800582
Max Magnitude0
OMIM111300
Desc
Variant0001
Relatedalso
ClinVar
Risk rs1800582(A;A)
Alt rs1800582(A;A)
Reference rs1800582(G;G)
Significance Pathogenic
Disease BLOOD GROUP ERIK
Variation info
Gene GYPA
CLNDBN BLOOD GROUP ERIK
Reversed 1
HGVS NC_000004.11:g.145040839C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000019288.27,