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rs45505091

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs45505091(A;T)
Make rs45505091(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271208
GeneHLA-C
is asnp
is mentioned by
dbSNPrs45505091
ebirs45505091
HLIrs45505091
Exacrs45505091
Varsomers45505091
Maprs45505091
PheGenIrs45505091
hapmaprs45505091
1000 genomesrs45505091
hgdprs45505091
ensemblrs45505091
gopubmedrs45505091
geneviewrs45505091
scholarrs45505091
googlers45505091
pharmgkbrs45505091
gwascentralrs45505091
openSNPrs45505091
23andMers45505091
23andMe allrs45505091
SNP Nexus

SNPshotrs45505091
SNPdbers45505091
MSV3drs45505091
GWAS Ctlgrs45505091
Max Magnitude0
ClinVar
Risk rs45505091(T;T)
Alt rs45505091(T;T)
Reference rs45505091(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238985T>A
CLNSRC
CLNACC