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rs28937582

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
(T;T) 0
Make rs28937582(A;C)
Make rs28937582(C;C)
ReferenceGRCh38 38.1/141
Chromosome3
Position161085958
GeneB3GALNT1
is asnp
is mentioned by
dbSNPrs28937582
ebirs28937582
HLIrs28937582
Exacrs28937582
Varsomers28937582
Maprs28937582
PheGenIrs28937582
hapmaprs28937582
1000 genomesrs28937582
hgdprs28937582
ensemblrs28937582
gopubmedrs28937582
geneviewrs28937582
scholarrs28937582
googlers28937582
pharmgkbrs28937582
gwascentralrs28937582
openSNPrs28937582
23andMers28937582
23andMe allrs28937582
SNP Nexus

SNPshotrs28937582
SNPdbers28937582
MSV3drs28937582
GWAS Ctlgrs28937582
Max Magnitude0
OMIM603094
DescBLOOD GROUP--P SYSTEM, P(k) ANTIGEN
Variant0004
Relatedalso


ClinVar
Risk rs28937582(C;C)
Alt rs28937582(C;C)
Reference rs28937582(A;A)
Significance Other
Disease p phenotype
Variation info
Gene B3GALNT1
CLNDBN p phenotype
Reversed 1
HGVS NC_000003.11:g.160803746T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000007015.3,