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rs181531333

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs181531333(C;T)
Make rs181531333(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271006
GeneHLA-C
is asnp
is mentioned by
dbSNPrs181531333
ebirs181531333
HLIrs181531333
Exacrs181531333
Varsomers181531333
Maprs181531333
PheGenIrs181531333
hapmaprs181531333
1000 genomesrs181531333
hgdprs181531333
ensemblrs181531333
gopubmedrs181531333
geneviewrs181531333
scholarrs181531333
googlers181531333
pharmgkbrs181531333
gwascentralrs181531333
openSNPrs181531333
23andMers181531333
23andMe allrs181531333
SNP Nexus

SNPshotrs181531333
SNPdbers181531333
MSV3drs181531333
GWAS Ctlgrs181531333
Max Magnitude0
ClinVar
Risk rs181531333(T;T)
Alt rs181531333(T;T)
Reference rs181531333(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31238783C>T
CLNSRC
CLNACC