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rs41551019

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41551019(C;G)
Make rs41551019(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271169
GeneHLA-C
is asnp
is mentioned by
dbSNPrs41551019
ebirs41551019
HLIrs41551019
Exacrs41551019
Varsomers41551019
Maprs41551019
PheGenIrs41551019
hapmaprs41551019
1000 genomesrs41551019
hgdprs41551019
ensemblrs41551019
gopubmedrs41551019
geneviewrs41551019
scholarrs41551019
googlers41551019
pharmgkbrs41551019
gwascentralrs41551019
openSNPrs41551019
23andMers41551019
23andMe allrs41551019
SNP Nexus

SNPshotrs41551019
SNPdbers41551019
MSV3drs41551019
GWAS Ctlgrs41551019
Max Magnitude0
ClinVar
Risk rs41551019(G,T;G,T)
Alt rs41551019(G,T;G,T)
Reference rs41551019(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238946G>A; NC_000006.11:g.31238946G>C
CLNSRC
CLNACC