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rs45465598

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs45465598(C;C)
Make rs45465598(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271195
GeneHLA-C
is asnp
is mentioned by
dbSNPrs45465598
ebirs45465598
HLIrs45465598
Exacrs45465598
Varsomers45465598
Maprs45465598
PheGenIrs45465598
hapmaprs45465598
1000 genomesrs45465598
hgdprs45465598
ensemblrs45465598
gopubmedrs45465598
geneviewrs45465598
scholarrs45465598
googlers45465598
pharmgkbrs45465598
gwascentralrs45465598
openSNPrs45465598
23andMers45465598
23andMe allrs45465598
SNP Nexus

SNPshotrs45465598
SNPdbers45465598
MSV3drs45465598
GWAS Ctlgrs45465598
Max Magnitude0
ClinVar
Risk rs45465598(C,G;C,G)
Alt rs45465598(C,G;C,G)
Reference rs45465598(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238972A>C
CLNSRC
CLNACC