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rs41556321

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41556321(A;A)
Make rs41556321(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270210
GeneHLA-C
is asnp
is mentioned by
dbSNPrs41556321
ebirs41556321
HLIrs41556321
Exacrs41556321
Varsomers41556321
Maprs41556321
PheGenIrs41556321
hapmaprs41556321
1000 genomesrs41556321
hgdprs41556321
ensemblrs41556321
gopubmedrs41556321
geneviewrs41556321
scholarrs41556321
googlers41556321
pharmgkbrs41556321
gwascentralrs41556321
openSNPrs41556321
23andMers41556321
23andMe allrs41556321
SNP Nexus

SNPshotrs41556321
SNPdbers41556321
MSV3drs41556321
GWAS Ctlgrs41556321
GMAF0.1185
Max Magnitude0
ClinVar
Risk rs41556321(A;A)
Alt rs41556321(A;A)
Reference rs41556321(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31237987C>T
CLNSRC
CLNACC