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rs121917779

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121917779(A;C)
Make rs121917779(C;C)
ReferenceGRCh38 38.1/141
Chromosome5
Position41201565
GeneC6
is asnp
is mentioned by
dbSNPrs121917779
ebirs121917779
HLIrs121917779
Exacrs121917779
Varsomers121917779
Maprs121917779
PheGenIrs121917779
hapmaprs121917779
1000 genomesrs121917779
hgdprs121917779
ensemblrs121917779
gopubmedrs121917779
geneviewrs121917779
scholarrs121917779
googlers121917779
pharmgkbrs121917779
gwascentralrs121917779
openSNPrs121917779
23andMers121917779
23andMe allrs121917779
SNP Nexus

SNPshotrs121917779
SNPdbers121917779
MSV3drs121917779
GWAS Ctlgrs121917779
Max Magnitude0
OMIM217050
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121917779(C,G;C,G)
Alt rs121917779(C,G;C,G)
Reference rs121917779(A;A)
Significance Non-pathogenic
Disease C6 A/B POLYMORPHISM
Variation info
Gene C6
CLNDBN C6 A/B POLYMORPHISM
Reversed 1
HGVS NC_000005.9:g.41201667T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000012896.2,