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rs41562320

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41562320(A;A)
Make rs41562320(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271286
GeneHLA-C
is asnp
is mentioned by
dbSNPrs41562320
ebirs41562320
HLIrs41562320
Exacrs41562320
Varsomers41562320
Maprs41562320
PheGenIrs41562320
hapmaprs41562320
1000 genomesrs41562320
hgdprs41562320
ensemblrs41562320
gopubmedrs41562320
geneviewrs41562320
scholarrs41562320
googlers41562320
pharmgkbrs41562320
gwascentralrs41562320
openSNPrs41562320
23andMers41562320
23andMe allrs41562320
SNP Nexus

SNPshotrs41562320
SNPdbers41562320
MSV3drs41562320
GWAS Ctlgrs41562320
Max Magnitude0
ClinVar
Risk rs41562320(A,C;A,C)
Alt rs41562320(A,C;A,C)
Reference rs41562320(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239063C>G; NC_000006.11:g.31239063C>T
CLNSRC
CLNACC