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rs3819287

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs3819287(A;A)
Make rs3819287(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31269786
GeneHLA-C
is asnp
is mentioned by
dbSNPrs3819287
ebirs3819287
HLIrs3819287
Exacrs3819287
Varsomers3819287
Maprs3819287
PheGenIrs3819287
hapmaprs3819287
1000 genomesrs3819287
hgdprs3819287
ensemblrs3819287
gopubmedrs3819287
geneviewrs3819287
scholarrs3819287
googlers3819287
pharmgkbrs3819287
gwascentralrs3819287
openSNPrs3819287
23andMers3819287
23andMe allrs3819287
SNP Nexus

SNPshotrs3819287
SNPdbers3819287
MSV3drs3819287
GWAS Ctlgrs3819287
GMAF0.2218
Max Magnitude0
ClinVar
Risk rs3819287(A;A)
Alt rs3819287(A;A)
Reference rs3819287(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31237563C>T
CLNSRC
CLNACC