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rs17199328

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs17199328(A;G)
Make rs17199328(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31354618
GeneHLA-B
is asnp
is mentioned by
dbSNPrs17199328
ebirs17199328
HLIrs17199328
Exacrs17199328
Varsomers17199328
Maprs17199328
PheGenIrs17199328
hapmaprs17199328
1000 genomesrs17199328
hgdprs17199328
ensemblrs17199328
gopubmedrs17199328
geneviewrs17199328
scholarrs17199328
googlers17199328
pharmgkbrs17199328
gwascentralrs17199328
openSNPrs17199328
23andMers17199328
23andMe allrs17199328
SNP Nexus

SNPshotrs17199328
SNPdbers17199328
MSV3drs17199328
GWAS Ctlgrs17199328
GMAF0.0877
Max Magnitude0
ClinVar
Risk rs17199328(G;G)
Alt rs17199328(G;G)
Reference rs17199328(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31322395A>G
CLNSRC
CLNACC