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rs1049650

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1049650(C;C)
Make rs1049650(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31269031
GeneHLA-C
is asnp
is mentioned by
dbSNPrs1049650
dbSNP (old)rs1049650
ClinGenrs1049650
ebirs1049650
HLIrs1049650
Exacrs1049650
Gnomadrs1049650
Varsomers1049650
Maprs1049650
PheGenIrs1049650
Biobankrs1049650
1000 genomesrs1049650
hgdprs1049650
ensemblrs1049650
gopubmedrs1049650
geneviewrs1049650
scholarrs1049650
googlers1049650
pharmgkbrs1049650
gwascentralrs1049650
openSNPrs1049650
23andMers1049650
23andMe allrs1049650
SNP Nexus

SNPshotrs1049650
SNPdbers1049650
MSV3drs1049650
GWAS Ctlgrs1049650
GMAF0.1244
Max Magnitude0
ClinVar
Risk rs1049650(C;C)
Alt rs1049650(C;C)
Reference Rs1049650(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31236808C>G
CLNSRC
CLNACC