rs767589799

Orientation

plus

Stabilized

plus

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

Make rs767589799(G;T)

Make rs767589799(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

9

Position

99149218

Gene

TGFBR1

is a	snp
is	mentioned by
dbSNP	rs767589799
dbSNP (classic)	rs767589799
ClinGen	rs767589799
ebi	rs767589799
HLI	rs767589799
Exac	rs767589799
Gnomad	rs767589799
Varsome	rs767589799
LitVar	rs767589799
Map	rs767589799
PheGenI	rs767589799
Biobank	rs767589799
1000 genomes	rs767589799
hgdp	rs767589799
ensembl	rs767589799
geneview	rs767589799
scholar	rs767589799
google	rs767589799
pharmgkb	rs767589799
gwascentral	rs767589799
openSNP	rs767589799
23andMe	rs767589799
SNPshot	rs767589799
SNPdbe	rs767589799
MSV3d	rs767589799
GWAS Ctlg	rs767589799

Max Magnitude

0

ClinVar
Risk	rs767589799(T;T)
Alt	rs767589799(T;T)
Reference	Rs767589799(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	TGFBR1
CLNDBN	not provided
Reversed	0
HGVS	NC_000009.11:g.101911500G>T
CLNSRC
CLNACC	RCV000490239.1,