rs200900510

Orientation

plus

Stabilized

plus

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

Make rs200900510(C;T)

Make rs200900510(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

12

Position

6329900

Gene

TNFRSF1A

is a	snp
is	mentioned by
dbSNP	rs200900510
dbSNP (classic)	rs200900510
ClinGen	rs200900510
ebi	rs200900510
HLI	rs200900510
Exac	rs200900510
Gnomad	rs200900510
Varsome	rs200900510
LitVar	rs200900510
Map	rs200900510
PheGenI	rs200900510
Biobank	rs200900510
1000 genomes	rs200900510
hgdp	rs200900510
ensembl	rs200900510
geneview	rs200900510
scholar	rs200900510
google	rs200900510
pharmgkb	rs200900510
gwascentral	rs200900510
openSNP	rs200900510
23andMe	rs200900510
SNPshot	rs200900510
SNPdbe	rs200900510
MSV3d	rs200900510
GWAS Ctlg	rs200900510

Max Magnitude

0

ClinVar
Risk	rs200900510(T;T)
Alt	rs200900510(T;T)
Reference	Rs200900510(C;C)
Significance	Pathogenic
Disease	not specified Behcet's syndrome
Variation	info
Gene	TNFRSF1A
CLNDBN	not specified Behcet's syndrome
Reversed	0
HGVS	NC_000012.11:g.6439066C>T
CLNSRC
CLNACC	RCV000419009.1, RCV000458191.1,