rs878854611

Orientation

plus

Stabilized

plus

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

Make rs878854611(-;-)

Make rs878854611(-;T)

Reference

GRCh38.p2 38.2/147

Chromosome

3

Position

30691424

Gene

TGFBR2

is a	snp
is	mentioned by
dbSNP	rs878854611
dbSNP (classic)	rs878854611
ClinGen	rs878854611
ebi	rs878854611
HLI	rs878854611
Exac	rs878854611
Gnomad	rs878854611
Varsome	rs878854611
LitVar	rs878854611
Map	rs878854611
PheGenI	rs878854611
Biobank	rs878854611
1000 genomes	rs878854611
hgdp	rs878854611
ensembl	rs878854611
geneview	rs878854611
scholar	rs878854611
google	rs878854611
pharmgkb	rs878854611
gwascentral	rs878854611
openSNP	rs878854611
23andMe	rs878854611
SNPshot	rs878854611
SNPdbe	rs878854611
MSV3d	rs878854611
GWAS Ctlg	rs878854611

Max Magnitude

0

ClinVar
Risk	rs878854611(-;-)
Alt	rs878854611(-;-)
Reference	Rs878854611(T;T)
Significance	Probable-Pathogenic
Disease	Thoracic aortic aneurysm and aortic dissection
Variation	info
Gene	TGFBR2
CLNDBN	Thoracic aortic aneurysm and aortic dissection
Reversed	0
HGVS	NC_000003.11:g.30732916delT
CLNSRC
CLNACC	RCV000227819.2,