Have questions? Visit https://www.reddit.com/r/SNPedia

rs45580333

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs45580333(A;A)
Make rs45580333(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271262
GeneHLA-C
is asnp
is mentioned by
dbSNPrs45580333
ebirs45580333
HLIrs45580333
Exacrs45580333
Varsomers45580333
Maprs45580333
PheGenIrs45580333
hapmaprs45580333
1000 genomesrs45580333
hgdprs45580333
ensemblrs45580333
gopubmedrs45580333
geneviewrs45580333
scholarrs45580333
googlers45580333
pharmgkbrs45580333
gwascentralrs45580333
openSNPrs45580333
23andMers45580333
23andMe allrs45580333
SNP Nexus

SNPshotrs45580333
SNPdbers45580333
MSV3drs45580333
GWAS Ctlgrs45580333
Max Magnitude0
ClinVar
Risk rs45580333(A,C,T;A,C,T)
Alt rs45580333(A,C,T;A,C,T)
Reference rs45580333(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239039C>A; NC_000006.11:g.31239039C>G; NC_000006.11:g.31239039C>T
CLNSRC
CLNACC