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rs151341100

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs151341100(A;A)
Make rs151341100(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271824
GeneHLA-C
is asnp
is mentioned by
dbSNPrs151341100
dbSNP (classic)rs151341100
ClinGenrs151341100
ebirs151341100
HLIrs151341100
Exacrs151341100
Gnomadrs151341100
Varsomers151341100
LitVarrs151341100
Maprs151341100
PheGenIrs151341100
Biobankrs151341100
1000 genomesrs151341100
hgdprs151341100
ensemblrs151341100
geneviewrs151341100
scholarrs151341100
googlers151341100
pharmgkbrs151341100
gwascentralrs151341100
openSNPrs151341100
23andMers151341100
SNPshotrs151341100
SNPdbers151341100
MSV3drs151341100
GWAS Ctlgrs151341100
Max Magnitude0
ClinVar
Risk rs151341100(A;A)
Alt rs151341100(A;A)
Reference Rs151341100(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324690C>T
CLNSRC
CLNACC