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rs1049853

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1049853(C;T)
Make rs1049853(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31269123
GeneHLA-C
is asnp
is mentioned by
dbSNPrs1049853
ebirs1049853
HLIrs1049853
Exacrs1049853
Varsomers1049853
Maprs1049853
PheGenIrs1049853
hapmaprs1049853
1000 genomesrs1049853
hgdprs1049853
ensemblrs1049853
gopubmedrs1049853
geneviewrs1049853
scholarrs1049853
googlers1049853
pharmgkbrs1049853
gwascentralrs1049853
openSNPrs1049853
23andMers1049853
23andMe allrs1049853
SNP Nexus

SNPshotrs1049853
SNPdbers1049853
MSV3drs1049853
GWAS Ctlgrs1049853
GMAF0.1125
Max Magnitude0
? (C;C) (C;T) (T;T) 28
ClinVar
Risk rs1049853(T;T)
Alt rs1049853(T;T)
Reference rs1049853(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31236900G>A
CLNSRC
CLNACC