rs2071888

Orientation

minus

Stabilized

minus

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

Make rs2071888(C;G)

Make rs2071888(G;G)

Reference

GRCh38 38.1/141

Chromosome

6

Position

33305078

Gene

TAPBP

is a	snp
is	mentioned by
dbSNP	rs2071888
dbSNP (classic)	rs2071888
ClinGen	rs2071888
ebi	rs2071888
HLI	rs2071888
Exac	rs2071888
Gnomad	rs2071888
Varsome	rs2071888
LitVar	rs2071888
Map	rs2071888
PheGenI	rs2071888
Biobank	rs2071888
1000 genomes	rs2071888
hgdp	rs2071888
ensembl	rs2071888
geneview	rs2071888
scholar	rs2071888
google	rs2071888
pharmgkb	rs2071888
gwascentral	rs2071888
openSNP	rs2071888
23andMe	rs2071888
SNPshot	rs2071888
SNPdbe	rs2071888
MSV3d	rs2071888
GWAS Ctlg	rs2071888

GMAF

0.4431

Max Magnitude

0

?	(C;C) (C;G) (G;G)	28

[PMID 24159917] Gastrointestinal stromal tumors: a case-only analysis of single nucleotide polymorphisms and somatic mutations

[PMID 20205905] Association of repeatedly measured intermediate risk factors for complex diseases with high dimensional SNP data.

[PMID 23736108] Association analysis of tapasin polymorphisms with aspirin-exacerbated respiratory disease in asthmatics.

ClinVar
Risk	rs2071888(G;G)
Alt	rs2071888(G;G)
Reference	Rs2071888(C;C)
Significance	Non-pathogenic
Disease	not specified
Variation	info
Gene	TAPBP
CLNDBN	not specified
Reversed	1
HGVS	NC_000006.11:g.33272855G>C
CLNSRC
CLNACC	RCV000455054.1,