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rs41551919

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41551919(A;A)
Make rs41551919(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356216
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41551919
ebirs41551919
HLIrs41551919
Exacrs41551919
Varsomers41551919
Maprs41551919
PheGenIrs41551919
hapmaprs41551919
1000 genomesrs41551919
hgdprs41551919
ensemblrs41551919
gopubmedrs41551919
geneviewrs41551919
scholarrs41551919
googlers41551919
pharmgkbrs41551919
gwascentralrs41551919
openSNPrs41551919
23andMers41551919
23andMe allrs41551919
SNP Nexus

SNPshotrs41551919
SNPdbers41551919
MSV3drs41551919
GWAS Ctlgrs41551919
Max Magnitude0
ClinVar
Risk rs41551919(A,C,T;A,C,T)
Alt rs41551919(A,C,T;A,C,T)
Reference rs41551919(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323993C>A; NC_000006.11:g.31323993C>G; NC_000006.11:g.31323993C>T
CLNSRC
CLNACC