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rs45558335

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs45558335(A;A)
Make rs45558335(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271302
GeneHLA-C
is asnp
is mentioned by
dbSNPrs45558335
ebirs45558335
HLIrs45558335
Exacrs45558335
Varsomers45558335
Maprs45558335
PheGenIrs45558335
hapmaprs45558335
1000 genomesrs45558335
hgdprs45558335
ensemblrs45558335
gopubmedrs45558335
geneviewrs45558335
scholarrs45558335
googlers45558335
pharmgkbrs45558335
gwascentralrs45558335
openSNPrs45558335
23andMers45558335
23andMe allrs45558335
SNP Nexus

SNPshotrs45558335
SNPdbers45558335
MSV3drs45558335
GWAS Ctlgrs45558335
Max Magnitude0
ClinVar
Risk rs45558335(A,G,T;A,G,T)
Alt rs45558335(A,G,T;A,G,T)
Reference rs45558335(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239079G>A; NC_000006.11:g.31239079G>C; NC_000006.11:g.31239079G>T
CLNSRC
CLNACC