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rs45622747

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs45622747(A;G)
Make rs45622747(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271196
GeneHLA-C
is asnp
is mentioned by
dbSNPrs45622747
ebirs45622747
HLIrs45622747
Exacrs45622747
Varsomers45622747
Maprs45622747
PheGenIrs45622747
hapmaprs45622747
1000 genomesrs45622747
hgdprs45622747
ensemblrs45622747
gopubmedrs45622747
geneviewrs45622747
scholarrs45622747
googlers45622747
pharmgkbrs45622747
gwascentralrs45622747
openSNPrs45622747
23andMers45622747
23andMe allrs45622747
SNP Nexus

SNPshotrs45622747
SNPdbers45622747
MSV3drs45622747
GWAS Ctlgrs45622747
Max Magnitude0
ClinVar
Risk rs45622747(G;G)
Alt rs45622747(G;G)
Reference rs45622747(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238973T>C
CLNSRC
CLNACC