rs7753873

Orientation

plus

Stabilized

plus

Make rs7753873(A;A)

Make rs7753873(A;C)

Make rs7753873(C;C)

Reference

GRCh38 38.1/141

Chromosome

6

Position

137852285

Gene	LOC100130476, LOC107986649

is a	snp
is	mentioned by
dbSNP	rs7753873
dbSNP (classic)	rs7753873
ClinGen	rs7753873
ebi	rs7753873
HLI	rs7753873
Exac	rs7753873
Gnomad	rs7753873
Varsome	rs7753873
LitVar	rs7753873
Map	rs7753873
PheGenI	rs7753873
Biobank	rs7753873
1000 genomes	rs7753873
hgdp	rs7753873
ensembl	rs7753873
geneview	rs7753873
scholar	rs7753873
google	rs7753873
pharmgkb	rs7753873
gwascentral	rs7753873
openSNP	rs7753873
23andMe	rs7753873
SNPshot	rs7753873
SNPdbe	rs7753873
MSV3d	rs7753873
GWAS Ctlg	rs7753873

GMAF

0.1708

Max Magnitude

0

?	(A;A) (A;C) (C;C)	28

[PMID 23161053] TNFAIP3 gene polymorphisms confer risk for Behcet's disease in a Chinese Han population