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

rs41545612

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41545612(A;A)
Make rs41545612(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356820
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41545612
ebirs41545612
HLIrs41545612
Exacrs41545612
Varsomers41545612
Maprs41545612
PheGenIrs41545612
hapmaprs41545612
1000 genomesrs41545612
hgdprs41545612
ensemblrs41545612
gopubmedrs41545612
geneviewrs41545612
scholarrs41545612
googlers41545612
pharmgkbrs41545612
gwascentralrs41545612
openSNPrs41545612
23andMers41545612
23andMe allrs41545612
SNP Nexus

SNPshotrs41545612
SNPdbers41545612
MSV3drs41545612
GWAS Ctlgrs41545612
Max Magnitude0
ClinVar
Risk rs41545612(A,T;A,T)
Alt rs41545612(A,T;A,T)
Reference rs41545612(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324597G>A; NC_000006.11:g.31324597G>T
CLNSRC
CLNACC