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rs56141211

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs56141211(A;A)
Make rs56141211(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position10626447
GeneGCNT2
is asnp
is mentioned by
dbSNPrs56141211
ebirs56141211
HLIrs56141211
Exacrs56141211
Varsomers56141211
Maprs56141211
PheGenIrs56141211
hapmaprs56141211
1000 genomesrs56141211
hgdprs56141211
ensemblrs56141211
gopubmedrs56141211
geneviewrs56141211
scholarrs56141211
googlers56141211
pharmgkbrs56141211
gwascentralrs56141211
openSNPrs56141211
23andMers56141211
23andMe allrs56141211
SNP Nexus

SNPshotrs56141211
SNPdbers56141211
MSV3drs56141211
GWAS Ctlgrs56141211
Max Magnitude0
OMIM600429
Desc
Variant0001
Relatedalso


ClinVar
Risk rs56141211(A;A)
Alt rs56141211(A;A)
Reference rs56141211(G;G)
Significance Pathogenic
Disease I blood group system
Variation info
Gene GCNT2
CLNDBN I blood group system
Reversed 0
HGVS NC_000006.11:g.10626680G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000009699.7,