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rs137853339

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137853339(A;A)
Make rs137853339(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position10529416
GeneGCNT2
is asnp
is mentioned by
dbSNPrs137853339
ebirs137853339
HLIrs137853339
Exacrs137853339
Varsomers137853339
Maprs137853339
PheGenIrs137853339
hapmaprs137853339
1000 genomesrs137853339
hgdprs137853339
ensemblrs137853339
gopubmedrs137853339
geneviewrs137853339
scholarrs137853339
googlers137853339
pharmgkbrs137853339
gwascentralrs137853339
openSNPrs137853339
23andMers137853339
23andMe allrs137853339
SNP Nexus

SNPshotrs137853339
SNPdbers137853339
MSV3drs137853339
GWAS Ctlgrs137853339
Max Magnitude0
OMIM600429
Desc
Variant0004
Relatedalso
ClinVar
Risk rs137853339(A;A)
Alt rs137853339(A;A)
Reference rs137853339(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.10529649G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000009702.8,