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rs45619135

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs45619135(A;A)
Make rs45619135(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271316
GeneHLA-C
is asnp
is mentioned by
dbSNPrs45619135
ebirs45619135
HLIrs45619135
Exacrs45619135
Varsomers45619135
Maprs45619135
PheGenIrs45619135
hapmaprs45619135
1000 genomesrs45619135
hgdprs45619135
ensemblrs45619135
gopubmedrs45619135
geneviewrs45619135
scholarrs45619135
googlers45619135
pharmgkbrs45619135
gwascentralrs45619135
openSNPrs45619135
23andMers45619135
23andMe allrs45619135
SNP Nexus

SNPshotrs45619135
SNPdbers45619135
MSV3drs45619135
GWAS Ctlgrs45619135
Max Magnitude0
ClinVar
Risk rs45619135(A,T;A,T)
Alt rs45619135(A,T;A,T)
Reference rs45619135(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239093C>A; NC_000006.11:g.31239093C>T
CLNSRC
CLNACC