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

rs41551415

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs41551415(G;G)
Make rs41551415(G;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355360
GeneHLA-B, MIR6891
is asnp
is mentioned by
dbSNPrs41551415
dbSNP (classic)rs41551415
ClinGenrs41551415
ebirs41551415
HLIrs41551415
Exacrs41551415
Gnomadrs41551415
Varsomers41551415
LitVarrs41551415
Maprs41551415
PheGenIrs41551415
Biobankrs41551415
1000 genomesrs41551415
hgdprs41551415
ensemblrs41551415
geneviewrs41551415
scholarrs41551415
googlers41551415
pharmgkbrs41551415
gwascentralrs41551415
openSNPrs41551415
23andMers41551415
SNPshotrs41551415
SNPdbers41551415
MSV3drs41551415
GWAS Ctlgrs41551415
Max Magnitude0
ClinVar
Risk rs41551415(G;G)
Alt rs41551415(G;G)
Reference Rs41551415(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323137A>C
CLNSRC
CLNACC