rs1071816

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(A;A)	0	common in clinvar

Make rs1071816(A;T)

Make rs1071816(T;T)

Reference

GRCh38 38.1/141

Chromosome

6

Position

31356759

Gene	HLA-B, MIR6891

is a	snp
is	mentioned by
dbSNP	rs1071816
dbSNP (classic)	rs1071816
ClinGen	rs1071816
ebi	rs1071816
HLI	rs1071816
Exac	rs1071816
Gnomad	rs1071816
Varsome	rs1071816
LitVar	rs1071816
Map	rs1071816
PheGenI	rs1071816
Biobank	rs1071816
1000 genomes	rs1071816
hgdp	rs1071816
ensembl	rs1071816
geneview	rs1071816
scholar	rs1071816
google	rs1071816
pharmgkb	rs1071816
gwascentral	rs1071816
openSNP	rs1071816
23andMe	rs1071816
SNPshot	rs1071816
SNPdbe	rs1071816
MSV3d	rs1071816
GWAS Ctlg	rs1071816

GMAF

0.4564

Max Magnitude

0

ClinVar
Risk	rs1071816(C;C) rs1071816(G;G) rs1071816(T;T)
Alt	rs1071816(C;C) rs1071816(G;G) rs1071816(T;T)
Reference	Rs1071816(A;A)
Significance	Histocompatibility
Disease
Variation	info
Gene	HLA-B
CLNDBN
Reversed	1
HGVS	NC_000006.11:g.31324536T>A; NC_000006.11:g.31324536T>C; NC_000006.11:g.31324536T>G
CLNSRC
CLNACC

[PMID 27157822] Genetic variants associated with antithyroid drug-induced agranulocytosis: a genome-wide association study in a European population.