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

rs3897530

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs3897530(A;A)
Make rs3897530(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355691
GeneHLA-B
is asnp
is mentioned by
dbSNPrs3897530
ebirs3897530
HLIrs3897530
Exacrs3897530
Varsomers3897530
Maprs3897530
PheGenIrs3897530
hapmaprs3897530
1000 genomesrs3897530
hgdprs3897530
ensemblrs3897530
gopubmedrs3897530
geneviewrs3897530
scholarrs3897530
googlers3897530
pharmgkbrs3897530
gwascentralrs3897530
openSNPrs3897530
23andMers3897530
23andMe allrs3897530
SNP Nexus

SNPshotrs3897530
SNPdbers3897530
MSV3drs3897530
GWAS Ctlgrs3897530
GMAF0.2603
Max Magnitude0
ClinVar
Risk rs3897530(A;A)
Alt rs3897530(A;A)
Reference rs3897530(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323468G>T
CLNSRC
CLNACC