rs869025533

Orientation

plus

Stabilized

plus

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

Make rs869025533(A;A)

Reference

GRCh38.p2 38.2/147

Chromosome

1

Position

218405192

Gene

TGFB2

is a	snp
is	mentioned by
dbSNP	rs869025533
dbSNP (classic)	rs869025533
ClinGen	rs869025533
ebi	rs869025533
HLI	rs869025533
Exac	rs869025533
Gnomad	rs869025533
Varsome	rs869025533
LitVar	rs869025533
Map	rs869025533
PheGenI	rs869025533
Biobank	rs869025533
1000 genomes	rs869025533
hgdp	rs869025533
ensembl	rs869025533
geneview	rs869025533
scholar	rs869025533
google	rs869025533
pharmgkb	rs869025533
gwascentral	rs869025533
openSNP	rs869025533
23andMe	rs869025533
SNPshot	rs869025533
SNPdbe	rs869025533
MSV3d	rs869025533
GWAS Ctlg	rs869025533

Max Magnitude

7

ClinVar
Risk	rs869025533(A;A)
Alt	rs869025533(A;A)
Reference	Rs869025533(-;-)
Significance	Probable-Pathogenic
Disease	Loeys-Dietz syndrome
Variation	info
Gene	TGFB2
CLNDBN	Loeys-Dietz syndrome
Reversed	0
HGVS	NC_000001.10:g.218578534dupA
CLNSRC
CLNACC	RCV000208163.1,