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

rs17193040

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs17193040(G;T)
Make rs17193040(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355026
GeneHLA-B, MIR6891
is asnp
is mentioned by
dbSNPrs17193040
dbSNP (classic)rs17193040
ClinGenrs17193040
ebirs17193040
HLIrs17193040
Exacrs17193040
Gnomadrs17193040
Varsomers17193040
LitVarrs17193040
Maprs17193040
PheGenIrs17193040
Biobankrs17193040
1000 genomesrs17193040
hgdprs17193040
ensemblrs17193040
geneviewrs17193040
scholarrs17193040
googlers17193040
pharmgkbrs17193040
gwascentralrs17193040
openSNPrs17193040
23andMers17193040
SNPshotrs17193040
SNPdbers17193040
MSV3drs17193040
GWAS Ctlgrs17193040
GMAF0.07392
Max Magnitude0
ClinVar
Risk rs17193040(C;C) rs17193040(T;T)
Alt rs17193040(C;C) rs17193040(T;T)
Reference Rs17193040(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31322803G>T
CLNSRC
CLNACC