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rs17199279

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs17199279(C;T)
Make rs17199279(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31354366
GeneHLA-B
is asnp
is mentioned by
dbSNPrs17199279
ebirs17199279
HLIrs17199279
Exacrs17199279
Varsomers17199279
Maprs17199279
PheGenIrs17199279
hapmaprs17199279
1000 genomesrs17199279
hgdprs17199279
ensemblrs17199279
gopubmedrs17199279
geneviewrs17199279
scholarrs17199279
googlers17199279
pharmgkbrs17199279
gwascentralrs17199279
openSNPrs17199279
23andMers17199279
23andMe allrs17199279
SNP Nexus

SNPshotrs17199279
SNPdbers17199279
MSV3drs17199279
GWAS Ctlgrs17199279
GMAF0.07392
Max Magnitude0
ClinVar
Risk rs17199279(T;T)
Alt rs17199279(T;T)
Reference rs17199279(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31322143C>T
CLNSRC
CLNACC