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rs55940927

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs55940927(A;A)
Make rs55940927(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position10626552
GeneGCNT2
is asnp
is mentioned by
dbSNPrs55940927
ebirs55940927
HLIrs55940927
Exacrs55940927
Varsomers55940927
Maprs55940927
PheGenIrs55940927
hapmaprs55940927
1000 genomesrs55940927
hgdprs55940927
ensemblrs55940927
gopubmedrs55940927
geneviewrs55940927
scholarrs55940927
googlers55940927
pharmgkbrs55940927
gwascentralrs55940927
openSNPrs55940927
23andMers55940927
23andMe allrs55940927
SNP Nexus

SNPshotrs55940927
SNPdbers55940927
MSV3drs55940927
GWAS Ctlgrs55940927
Max Magnitude0
OMIM600429
Desc
Variant0002
Relatedalso
ClinVar
Risk rs55940927(A;A)
Alt rs55940927(A;A)
Reference rs55940927(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.10626785G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000009700.7,