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

rs137854723

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs137854723(A;T)
Make rs137854723(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356373
GeneHLA-B
is asnp
is mentioned by
dbSNPrs137854723
ebirs137854723
HLIrs137854723
Exacrs137854723
Varsomers137854723
Maprs137854723
PheGenIrs137854723
hapmaprs137854723
1000 genomesrs137854723
hgdprs137854723
ensemblrs137854723
gopubmedrs137854723
geneviewrs137854723
scholarrs137854723
googlers137854723
pharmgkbrs137854723
gwascentralrs137854723
openSNPrs137854723
23andMers137854723
23andMe allrs137854723
SNP Nexus

SNPshotrs137854723
SNPdbers137854723
MSV3drs137854723
GWAS Ctlgrs137854723
Max Magnitude0
ClinVar
Risk rs137854723(G,T;G,T)
Alt rs137854723(G,T;G,T)
Reference rs137854723(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324150T>A; NC_000006.11:g.31324150T>C
CLNSRC
CLNACC