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rs3819305

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs3819305(C;C)
Make rs3819305(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31354367
GeneHLA-B
is asnp
is mentioned by
dbSNPrs3819305
dbSNP (classic)rs3819305
ClinGenrs3819305
ebirs3819305
HLIrs3819305
Exacrs3819305
Gnomadrs3819305
Varsomers3819305
LitVarrs3819305
Maprs3819305
PheGenIrs3819305
Biobankrs3819305
1000 genomesrs3819305
hgdprs3819305
ensemblrs3819305
geneviewrs3819305
scholarrs3819305
googlers3819305
pharmgkbrs3819305
gwascentralrs3819305
openSNPrs3819305
23andMers3819305
SNPshotrs3819305
SNPdbers3819305
MSV3drs3819305
GWAS Ctlgrs3819305
GMAF0.3567
Max Magnitude0
ClinVar
Risk rs3819305(C;C)
Alt rs3819305(C;C)
Reference Rs3819305(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31322144C>G
CLNSRC
CLNACC