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rs45501796

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs45501796(A;G)
Make rs45501796(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271619
GeneHLA-C
is asnp
is mentioned by
dbSNPrs45501796
ebirs45501796
HLIrs45501796
Exacrs45501796
Varsomers45501796
Maprs45501796
PheGenIrs45501796
hapmaprs45501796
1000 genomesrs45501796
hgdprs45501796
ensemblrs45501796
gopubmedrs45501796
geneviewrs45501796
scholarrs45501796
googlers45501796
pharmgkbrs45501796
gwascentralrs45501796
openSNPrs45501796
23andMers45501796
23andMe allrs45501796
SNP Nexus

SNPshotrs45501796
SNPdbers45501796
MSV3drs45501796
GWAS Ctlgrs45501796
Max Magnitude0
ClinVar
Risk rs45501796(G;G)
Alt rs45501796(G;G)
Reference rs45501796(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239396T>C
CLNSRC
CLNACC