rs863223814

Orientation

plus

Stabilized

plus

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

Make rs863223814(C;C)

Make rs863223814(C;T)

Reference

GRCh38.p2 38.2/146

Chromosome

9

Position

99138008

Gene

TGFBR1

is a	snp
is	mentioned by
dbSNP	rs863223814
dbSNP (classic)	rs863223814
ClinGen	rs863223814
ebi	rs863223814
HLI	rs863223814
Exac	rs863223814
Gnomad	rs863223814
Varsome	rs863223814
LitVar	rs863223814
Map	rs863223814
PheGenI	rs863223814
Biobank	rs863223814
1000 genomes	rs863223814
hgdp	rs863223814
ensembl	rs863223814
geneview	rs863223814
scholar	rs863223814
google	rs863223814
pharmgkb	rs863223814
gwascentral	rs863223814
openSNP	rs863223814
23andMe	rs863223814
SNPshot	rs863223814
SNPdbe	rs863223814
MSV3d	rs863223814
GWAS Ctlg	rs863223814

Max Magnitude

0

ClinVar
Risk	rs863223814(C;C)
Alt	rs863223814(C;C)
Reference	Rs863223814(T;T)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	TGFBR1
CLNDBN	not provided
Reversed	0
HGVS	NC_000009.11:g.101900290T>C
CLNSRC
CLNACC	RCV000200391.1,