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

rs41556514

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41556514(C;G)
Make rs41556514(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356298
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41556514
ebirs41556514
HLIrs41556514
Exacrs41556514
Varsomers41556514
Maprs41556514
PheGenIrs41556514
hapmaprs41556514
1000 genomesrs41556514
hgdprs41556514
ensemblrs41556514
gopubmedrs41556514
geneviewrs41556514
scholarrs41556514
googlers41556514
pharmgkbrs41556514
gwascentralrs41556514
openSNPrs41556514
23andMers41556514
23andMe allrs41556514
SNP Nexus

SNPshotrs41556514
SNPdbers41556514
MSV3drs41556514
GWAS Ctlgrs41556514
Max Magnitude0
ClinVar
Risk rs41556514(G,T;G,T)
Alt rs41556514(G,T;G,T)
Reference rs41556514(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324075G>A; NC_000006.11:g.31324075G>C
CLNSRC
CLNACC