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rs41562518

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41562518(A;A)
Make rs41562518(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271217
GeneHLA-C
is asnp
is mentioned by
dbSNPrs41562518
ebirs41562518
HLIrs41562518
Exacrs41562518
Varsomers41562518
Maprs41562518
PheGenIrs41562518
hapmaprs41562518
1000 genomesrs41562518
hgdprs41562518
ensemblrs41562518
gopubmedrs41562518
geneviewrs41562518
scholarrs41562518
googlers41562518
pharmgkbrs41562518
gwascentralrs41562518
openSNPrs41562518
23andMers41562518
23andMe allrs41562518
SNP Nexus

SNPshotrs41562518
SNPdbers41562518
MSV3drs41562518
GWAS Ctlgrs41562518
Max Magnitude0
ClinVar
Risk rs41562518(A,C;A,C)
Alt rs41562518(A,C;A,C)
Reference rs41562518(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238994C>G; NC_000006.11:g.31238994C>T
CLNSRC
CLNACC