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rs28940571

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
(G;G) 0
Make rs28940571(C;T)
Make rs28940571(T;T)
ReferenceGRCh38 38.1/141
Chromosome22
Position42693200
GeneA4GALT
is asnp
is mentioned by
dbSNPrs28940571
ebirs28940571
HLIrs28940571
Exacrs28940571
Varsomers28940571
Maprs28940571
PheGenIrs28940571
hapmaprs28940571
1000 genomesrs28940571
hgdprs28940571
ensemblrs28940571
gopubmedrs28940571
geneviewrs28940571
scholarrs28940571
googlers28940571
pharmgkbrs28940571
gwascentralrs28940571
openSNPrs28940571
23andMers28940571
23andMe allrs28940571
SNP Nexus

SNPshotrs28940571
SNPdbers28940571
MSV3drs28940571
GWAS Ctlgrs28940571
GMAF0.0004591
Max Magnitude0
OMIM607922
DescP BLOOD GROUP SYSTEM, p PHENOTYPE
Variant0002
Relatedalso
Neighborrs28940572
Distance192


ClinVar
Risk rs28940571(A,T;A,T)
Alt rs28940571(A,T;A,T)
Reference rs28940571(C;C)
Significance Other
Disease p phenotype
Variation info
Gene A4GALT
CLNDBN p phenotype
Reversed 1
HGVS NC_000022.10:g.43089206G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000002812.3,