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

rs41564319

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41564319(A;A)
Make rs41564319(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356886
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41564319
ebirs41564319
HLIrs41564319
Exacrs41564319
Varsomers41564319
Maprs41564319
PheGenIrs41564319
hapmaprs41564319
1000 genomesrs41564319
hgdprs41564319
ensemblrs41564319
gopubmedrs41564319
geneviewrs41564319
scholarrs41564319
googlers41564319
pharmgkbrs41564319
gwascentralrs41564319
openSNPrs41564319
23andMers41564319
23andMe allrs41564319
SNP Nexus

SNPshotrs41564319
SNPdbers41564319
MSV3drs41564319
GWAS Ctlgrs41564319
Max Magnitude0
ClinVar
Risk rs41564319(A;A)
Alt rs41564319(A;A)
Reference rs41564319(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324663C>T
CLNSRC
CLNACC