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rs41545014

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41545014(C;T)
Make rs41545014(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270437
GeneHLA-C
is asnp
is mentioned by
dbSNPrs41545014
ebirs41545014
HLIrs41545014
Exacrs41545014
Varsomers41545014
Maprs41545014
PheGenIrs41545014
hapmaprs41545014
1000 genomesrs41545014
hgdprs41545014
ensemblrs41545014
gopubmedrs41545014
geneviewrs41545014
scholarrs41545014
googlers41545014
pharmgkbrs41545014
gwascentralrs41545014
openSNPrs41545014
23andMers41545014
23andMe allrs41545014
SNP Nexus

SNPshotrs41545014
SNPdbers41545014
MSV3drs41545014
GWAS Ctlgrs41545014
Max Magnitude0
ClinVar
Risk rs41545014(T;T)
Alt rs41545014(T;T)
Reference rs41545014(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238214G>A
CLNSRC
CLNACC