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rs41545214

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41545214(C;G)
Make rs41545214(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270181
GeneHLA-C
is asnp
is mentioned by
dbSNPrs41545214
ebirs41545214
HLIrs41545214
Exacrs41545214
Varsomers41545214
Maprs41545214
PheGenIrs41545214
hapmaprs41545214
1000 genomesrs41545214
hgdprs41545214
ensemblrs41545214
gopubmedrs41545214
geneviewrs41545214
scholarrs41545214
googlers41545214
pharmgkbrs41545214
gwascentralrs41545214
openSNPrs41545214
23andMers41545214
23andMe allrs41545214
SNP Nexus

SNPshotrs41545214
SNPdbers41545214
MSV3drs41545214
GWAS Ctlgrs41545214
Max Magnitude0
ClinVar
Risk rs41545214(G;G)
Alt rs41545214(G;G)
Reference rs41545214(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31237958G>C
CLNSRC
CLNACC