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

rs4997052

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs4997052(A;A)
Make rs4997052(A;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356367
GeneHLA-B
is asnp
is mentioned by
dbSNPrs4997052
ebirs4997052
HLIrs4997052
Exacrs4997052
Varsomers4997052
Maprs4997052
PheGenIrs4997052
hapmaprs4997052
1000 genomesrs4997052
hgdprs4997052
ensemblrs4997052
gopubmedrs4997052
geneviewrs4997052
scholarrs4997052
googlers4997052
pharmgkbrs4997052
gwascentralrs4997052
openSNPrs4997052
23andMers4997052
23andMe allrs4997052
SNP Nexus

SNPshotrs4997052
SNPdbers4997052
MSV3drs4997052
GWAS Ctlgrs4997052
Max Magnitude0
ClinVar
Risk rs4997052(A,G;A,G)
Alt rs4997052(A,G;A,G)
Reference rs4997052(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31324144T>A; NC_000006.11:g.31324144T>G
CLNSRC
CLNACC


[PMID 20679961] Development of new HLA-B*3505 genotyping method using Invader assay.