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rs45597335

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs45597335(A;A)
Make rs45597335(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271194
GeneHLA-C
is asnp
is mentioned by
dbSNPrs45597335
ebirs45597335
HLIrs45597335
Exacrs45597335
Varsomers45597335
Maprs45597335
PheGenIrs45597335
hapmaprs45597335
1000 genomesrs45597335
hgdprs45597335
ensemblrs45597335
gopubmedrs45597335
geneviewrs45597335
scholarrs45597335
googlers45597335
pharmgkbrs45597335
gwascentralrs45597335
openSNPrs45597335
23andMers45597335
23andMe allrs45597335
SNP Nexus

SNPshotrs45597335
SNPdbers45597335
MSV3drs45597335
GWAS Ctlgrs45597335
Max Magnitude0
ClinVar
Risk rs45597335(A,G,T;A,G,T)
Alt rs45597335(A,G,T;A,G,T)
Reference rs45597335(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238971G>A; NC_000006.11:g.31238971G>C; NC_000006.11:g.31238971G>T
CLNSRC
CLNACC