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

rs41562117

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs41562117(A;G)
Make rs41562117(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355152
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41562117
ebirs41562117
HLIrs41562117
Exacrs41562117
Varsomers41562117
Maprs41562117
PheGenIrs41562117
hapmaprs41562117
1000 genomesrs41562117
hgdprs41562117
ensemblrs41562117
gopubmedrs41562117
geneviewrs41562117
scholarrs41562117
googlers41562117
pharmgkbrs41562117
gwascentralrs41562117
openSNPrs41562117
23andMers41562117
23andMe allrs41562117
SNP Nexus

SNPshotrs41562117
SNPdbers41562117
MSV3drs41562117
GWAS Ctlgrs41562117
Max Magnitude0
ClinVar
Risk rs41562117(G;G)
Alt rs41562117(G;G)
Reference rs41562117(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31322929T>C
CLNSRC
CLNACC