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rs80060802

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs80060802(C;G)
Make rs80060802(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355566
GeneHLA-B
is asnp
is mentioned by
dbSNPrs80060802
ebirs80060802
HLIrs80060802
Exacrs80060802
Varsomers80060802
Maprs80060802
PheGenIrs80060802
hapmaprs80060802
1000 genomesrs80060802
hgdprs80060802
ensemblrs80060802
gopubmedrs80060802
geneviewrs80060802
scholarrs80060802
googlers80060802
pharmgkbrs80060802
gwascentralrs80060802
openSNPrs80060802
23andMers80060802
23andMe allrs80060802
SNP Nexus

SNPshotrs80060802
SNPdbers80060802
MSV3drs80060802
GWAS Ctlgrs80060802
Max Magnitude0
ClinVar
Risk rs80060802(G;G)
Alt rs80060802(G;G)
Reference rs80060802(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323343G>C
CLNSRC
CLNACC