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rs113324237

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs113324237(G;T)
Make rs113324237(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29943635
GeneHLA-A
is asnp
is mentioned by
dbSNPrs113324237
ebirs113324237
HLIrs113324237
Exacrs113324237
Varsomers113324237
Maprs113324237
PheGenIrs113324237
hapmaprs113324237
1000 genomesrs113324237
hgdprs113324237
ensemblrs113324237
gopubmedrs113324237
geneviewrs113324237
scholarrs113324237
googlers113324237
pharmgkbrs113324237
gwascentralrs113324237
openSNPrs113324237
23andMers113324237
23andMe allrs113324237
SNP Nexus

SNPshotrs113324237
SNPdbers113324237
MSV3drs113324237
GWAS Ctlgrs113324237
Max Magnitude0
ClinVar
Risk rs113324237(T;T)
Alt rs113324237(T;T)
Reference rs113324237(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29911412G>T
CLNSRC
CLNACC