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

rs41560712

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41560712(C;C)
Make rs41560712(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356426
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41560712
ebirs41560712
HLIrs41560712
Exacrs41560712
Varsomers41560712
Maprs41560712
PheGenIrs41560712
hapmaprs41560712
1000 genomesrs41560712
hgdprs41560712
ensemblrs41560712
gopubmedrs41560712
geneviewrs41560712
scholarrs41560712
googlers41560712
pharmgkbrs41560712
gwascentralrs41560712
openSNPrs41560712
23andMers41560712
23andMe allrs41560712
SNP Nexus

SNPshotrs41560712
SNPdbers41560712
MSV3drs41560712
GWAS Ctlgrs41560712
Max Magnitude0
ClinVar
Risk rs41560712(C;C)
Alt rs41560712(C;C)
Reference rs41560712(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324203C>G
CLNSRC
CLNACC