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rs17193012

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs17193012(C;T)
Make rs17193012(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31354926
GeneHLA-B
is asnp
is mentioned by
dbSNPrs17193012
ebirs17193012
HLIrs17193012
Exacrs17193012
Varsomers17193012
Maprs17193012
PheGenIrs17193012
hapmaprs17193012
1000 genomesrs17193012
hgdprs17193012
ensemblrs17193012
gopubmedrs17193012
geneviewrs17193012
scholarrs17193012
googlers17193012
pharmgkbrs17193012
gwascentralrs17193012
openSNPrs17193012
23andMers17193012
23andMe allrs17193012
SNP Nexus

SNPshotrs17193012
SNPdbers17193012
MSV3drs17193012
GWAS Ctlgrs17193012
Max Magnitude0
ClinVar
Risk rs17193012(T;T)
Alt rs17193012(T;T)
Reference rs17193012(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31322703C>T
CLNSRC
CLNACC