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rs28940572

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0
(G;G) 0 common in clinvar
Make rs28940572(A;A)
Make rs28940572(A;G)
ReferenceGRCh38 38.1/141
Chromosome22
Position42693392
GeneA4GALT
is asnp
is mentioned by
dbSNPrs28940572
ebirs28940572
HLIrs28940572
Exacrs28940572
Varsomers28940572
Maprs28940572
PheGenIrs28940572
hapmaprs28940572
1000 genomesrs28940572
hgdprs28940572
ensemblrs28940572
gopubmedrs28940572
geneviewrs28940572
scholarrs28940572
googlers28940572
pharmgkbrs28940572
gwascentralrs28940572
openSNPrs28940572
23andMers28940572
23andMe allrs28940572
SNP Nexus

SNPshotrs28940572
SNPdbers28940572
MSV3drs28940572
GWAS Ctlgrs28940572
Max Magnitude0
OMIM607922
DescP BLOOD GROUP SYSTEM, p PHENOTYPE
Variant0004
Relatedalso
Neighborrs28940571
Distance192


ClinVar
Risk rs28940572(A;A)
Alt rs28940572(A;A)
Reference rs28940572(G;G)
Significance Other
Disease p phenotype
Variation info
Gene A4GALT
CLNDBN p phenotype
Reversed 1
HGVS NC_000022.10:g.43089398C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000002814.3,