rs886039866

Orientation

minus

Stabilized

minus

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

Make rs886039866(C;T)

Make rs886039866(T;T)

Reference

GRCh38.p7 38.3/149

Chromosome

12

Position

6333376

Gene

TNFRSF1A

is a	snp
is	mentioned by
dbSNP	rs886039866
dbSNP (classic)	rs886039866
ClinGen	rs886039866
ebi	rs886039866
HLI	rs886039866
Exac	rs886039866
Gnomad	rs886039866
Varsome	rs886039866
LitVar	rs886039866
Map	rs886039866
PheGenI	rs886039866
Biobank	rs886039866
1000 genomes	rs886039866
hgdp	rs886039866
ensembl	rs886039866
geneview	rs886039866
scholar	rs886039866
google	rs886039866
pharmgkb	rs886039866
gwascentral	rs886039866
openSNP	rs886039866
23andMe	rs886039866
SNPshot	rs886039866
SNPdbe	rs886039866
MSV3d	rs886039866
GWAS Ctlg	rs886039866

Max Magnitude

0

ClinVar
Risk	rs886039866(T;T)
Alt	rs886039866(T;T)
Reference	Rs886039866(C;C)
Significance	Pathogenic
Disease	Behcet's syndrome
Variation	info
Gene	TNFRSF1A
CLNDBN	Behcet's syndrome
Reversed	1
HGVS	NC_000012.11:g.6442542G>A
CLNSRC
CLNACC	RCV000258049.1,