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rs41543517

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41543517(A;A)
Make rs41543517(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271129
GeneHLA-C
is asnp
is mentioned by
dbSNPrs41543517
ebirs41543517
HLIrs41543517
Exacrs41543517
Varsomers41543517
Maprs41543517
PheGenIrs41543517
hapmaprs41543517
1000 genomesrs41543517
hgdprs41543517
ensemblrs41543517
gopubmedrs41543517
geneviewrs41543517
scholarrs41543517
googlers41543517
pharmgkbrs41543517
gwascentralrs41543517
openSNPrs41543517
23andMers41543517
23andMe allrs41543517
SNP Nexus

SNPshotrs41543517
SNPdbers41543517
MSV3drs41543517
GWAS Ctlgrs41543517
Max Magnitude0
ClinVar
Risk rs41543517(A,C,T;A,C,T)
Alt rs41543517(A,C,T;A,C,T)
Reference rs41543517(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238906C>A; NC_000006.11:g.31238906C>G; NC_000006.11:g.31238906C>T
CLNSRC
CLNACC