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rs41549514

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41549514(A;A)
Make rs41549514(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271647
GeneHLA-C
is asnp
is mentioned by
dbSNPrs41549514
ebirs41549514
HLIrs41549514
Exacrs41549514
Varsomers41549514
Maprs41549514
PheGenIrs41549514
hapmaprs41549514
1000 genomesrs41549514
hgdprs41549514
ensemblrs41549514
gopubmedrs41549514
geneviewrs41549514
scholarrs41549514
googlers41549514
pharmgkbrs41549514
gwascentralrs41549514
openSNPrs41549514
23andMers41549514
23andMe allrs41549514
SNP Nexus

SNPshotrs41549514
SNPdbers41549514
MSV3drs41549514
GWAS Ctlgrs41549514
Max Magnitude0
ClinVar
Risk rs41549514(A,G,T;A,G,T)
Alt rs41549514(A,G,T;A,G,T)
Reference rs41549514(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239424G>A; NC_000006.11:g.31239424G>C; NC_000006.11:g.31239424G>T
CLNSRC
CLNACC