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rs137854699

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137854699(A;A)
Make rs137854699(A;G)
ReferenceGRCh37.p5 37.3/137
Chromosome6
Position31324219
GeneHLA-B
is asnp
is mentioned by
dbSNPrs137854699
ebirs137854699
HLIrs137854699
Exacrs137854699
Varsomers137854699
Maprs137854699
PheGenIrs137854699
hapmaprs137854699
1000 genomesrs137854699
hgdprs137854699
ensemblrs137854699
gopubmedrs137854699
geneviewrs137854699
scholarrs137854699
googlers137854699
pharmgkbrs137854699
gwascentralrs137854699
openSNPrs137854699
23andMers137854699
23andMe allrs137854699
SNP Nexus

SNPshotrs137854699
SNPdbers137854699
MSV3drs137854699
GWAS Ctlgrs137854699
StatusDeleted
Max Magnitude0
ClinVar
Risk rs137854699(A,C;A,C)
Alt rs137854699(A,C;A,C)
Reference rs137854699(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324219C>G; NC_000006.11:g.31324219C>T
CLNSRC
CLNACC