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rs137853340

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137853340(A;A)
Make rs137853340(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position10529594
GeneGCNT2
is asnp
is mentioned by
dbSNPrs137853340
ebirs137853340
HLIrs137853340
Exacrs137853340
Varsomers137853340
Maprs137853340
PheGenIrs137853340
hapmaprs137853340
1000 genomesrs137853340
hgdprs137853340
ensemblrs137853340
gopubmedrs137853340
geneviewrs137853340
scholarrs137853340
googlers137853340
pharmgkbrs137853340
gwascentralrs137853340
openSNPrs137853340
23andMers137853340
23andMe allrs137853340
SNP Nexus

SNPshotrs137853340
SNPdbers137853340
MSV3drs137853340
GWAS Ctlgrs137853340
Max Magnitude0
OMIM600429
Desc
Variant0005
Relatedalso
ClinVar
Risk rs137853340(A;A)
Alt rs137853340(A;A)
Reference rs137853340(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.10529827G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000009703.10,