rs587776770

Orientation

plus

Stabilized

plus

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

Make rs587776770(G;G)

Reference

GRCh38 38.1/142

Chromosome

3

Position

30688382

Gene

TGFBR2

is a	snp
is	mentioned by
dbSNP	rs587776770
dbSNP (classic)	rs587776770
ClinGen	rs587776770
ebi	rs587776770
HLI	rs587776770
Exac	rs587776770
Gnomad	rs587776770
Varsome	rs587776770
LitVar	rs587776770
Map	rs587776770
PheGenI	rs587776770
Biobank	rs587776770
1000 genomes	rs587776770
hgdp	rs587776770
ensembl	rs587776770
geneview	rs587776770
scholar	rs587776770
google	rs587776770
pharmgkb	rs587776770
gwascentral	rs587776770
openSNP	rs587776770
23andMe	rs587776770
SNPshot	rs587776770
SNPdbe	rs587776770
MSV3d	rs587776770
GWAS Ctlg	rs587776770

Max Magnitude

7

ClinVar
Risk	rs587776770(G;G)
Alt	rs587776770(G;G)
Reference	Rs587776770(A;A)
Significance	Pathogenic
Disease	Loeys-Dietz syndrome 2
Variation	info
Gene	TGFBR2
CLNDBN	Loeys-Dietz syndrome 2
Reversed	0
HGVS	NC_000003.11:g.30729874A>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000013341.17,