rs759805984

Orientation

plus

Stabilized

plus

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

Make rs759805984(A;A)

Make rs759805984(A;T)

Reference

GRCh38.p2 38.2/146

Chromosome

9

Position

99149213

Gene

TGFBR1

is a	snp
is	mentioned by
dbSNP	rs759805984
dbSNP (classic)	rs759805984
ClinGen	rs759805984
ebi	rs759805984
HLI	rs759805984
Exac	rs759805984
Gnomad	rs759805984
Varsome	rs759805984
LitVar	rs759805984
Map	rs759805984
PheGenI	rs759805984
Biobank	rs759805984
1000 genomes	rs759805984
hgdp	rs759805984
ensembl	rs759805984
geneview	rs759805984
scholar	rs759805984
google	rs759805984
pharmgkb	rs759805984
gwascentral	rs759805984
openSNP	rs759805984
23andMe	rs759805984
SNPshot	rs759805984
SNPdbe	rs759805984
MSV3d	rs759805984
GWAS Ctlg	rs759805984

Max Magnitude

0

ClinVar
Risk	rs759805984(A;A) rs759805984(C;C)
Alt	rs759805984(A;A) rs759805984(C;C)
Reference	Rs759805984(T;T)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	TGFBR1
CLNDBN	not provided
Reversed	0
HGVS	NC_000009.11:g.101911495T>C
CLNSRC
CLNACC	RCV000198521.1,