rs587782979

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(A;G)	7	Loeys-Dietz Syndrome
(G;G)	0	common in clinvar

Make rs587782979(A;A)

Reference

GRCh38.p2 38.2/144

Chromosome

3

Position

30674232

Gene

TGFBR2

is a	snp
is	mentioned by
dbSNP	rs587782979
dbSNP (classic)	rs587782979
ClinGen	rs587782979
ebi	rs587782979
HLI	rs587782979
Exac	rs587782979
Gnomad	rs587782979
Varsome	rs587782979
LitVar	rs587782979
Map	rs587782979
PheGenI	rs587782979
Biobank	rs587782979
1000 genomes	rs587782979
hgdp	rs587782979
ensembl	rs587782979
geneview	rs587782979
scholar	rs587782979
google	rs587782979
pharmgkb	rs587782979
gwascentral	rs587782979
openSNP	rs587782979
23andMe	rs587782979
SNPshot	rs587782979
SNPdbe	rs587782979
MSV3d	rs587782979
GWAS Ctlg	rs587782979

Max Magnitude

7

ClinVar
Risk	rs587782979(A;A)
Alt	rs587782979(A;A)
Reference	Rs587782979(G;G)
Significance	Probable-Pathogenic
Disease	Loeys-Dietz syndrome
Variation	info
Gene	TGFBR2
CLNDBN	Loeys-Dietz syndrome
Reversed	0
HGVS	NC_000003.11:g.30715724G>A
CLNSRC
CLNACC	RCV000143955.1,