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

rs41551514

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs41551514(A;G)
Make rs41551514(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356099
GeneHLA-B, MIR6891
is asnp
is mentioned by
dbSNPrs41551514
dbSNP (classic)rs41551514
ClinGenrs41551514
ebirs41551514
HLIrs41551514
Exacrs41551514
Gnomadrs41551514
Varsomers41551514
LitVarrs41551514
Maprs41551514
PheGenIrs41551514
Biobankrs41551514
1000 genomesrs41551514
hgdprs41551514
ensemblrs41551514
geneviewrs41551514
scholarrs41551514
googlers41551514
pharmgkbrs41551514
gwascentralrs41551514
openSNPrs41551514
23andMers41551514
SNPshotrs41551514
SNPdbers41551514
MSV3drs41551514
GWAS Ctlgrs41551514
Max Magnitude0
ClinVar
Risk rs41551514(G;G)
Alt rs41551514(G;G)
Reference Rs41551514(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323876T>C
CLNSRC
CLNACC