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

rs140505137

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs140505137(A;A)
Make rs140505137(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270546
GeneHLA-C
is asnp
is mentioned by
dbSNPrs140505137
ebirs140505137
HLIrs140505137
Exacrs140505137
Varsomers140505137
Maprs140505137
PheGenIrs140505137
hapmaprs140505137
1000 genomesrs140505137
hgdprs140505137
ensemblrs140505137
gopubmedrs140505137
geneviewrs140505137
scholarrs140505137
googlers140505137
pharmgkbrs140505137
gwascentralrs140505137
openSNPrs140505137
23andMers140505137
23andMe allrs140505137
SNP Nexus

SNPshotrs140505137
SNPdbers140505137
MSV3drs140505137
GWAS Ctlgrs140505137
GMAF0.004132
Max Magnitude0
ClinVar
Risk rs140505137(A;A)
Alt rs140505137(A;A)
Reference rs140505137(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31238323G>A
CLNSRC
CLNACC