rs863223812

Orientation

plus

Stabilized

plus

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

Make rs863223812(C;T)

Make rs863223812(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

9

Position

99137991

Gene

TGFBR1

is a	snp
is	mentioned by
dbSNP	rs863223812
dbSNP (classic)	rs863223812
ClinGen	rs863223812
ebi	rs863223812
HLI	rs863223812
Exac	rs863223812
Gnomad	rs863223812
Varsome	rs863223812
LitVar	rs863223812
Map	rs863223812
PheGenI	rs863223812
Biobank	rs863223812
1000 genomes	rs863223812
hgdp	rs863223812
ensembl	rs863223812
geneview	rs863223812
scholar	rs863223812
google	rs863223812
pharmgkb	rs863223812
gwascentral	rs863223812
openSNP	rs863223812
23andMe	rs863223812
SNPshot	rs863223812
SNPdbe	rs863223812
MSV3d	rs863223812
GWAS Ctlg	rs863223812

Max Magnitude

0

ClinVar
Risk	rs863223812(T;T)
Alt	rs863223812(T;T)
Reference	Rs863223812(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	TGFBR1
CLNDBN	not provided
Reversed	0
HGVS	NC_000009.11:g.101900273C>T
CLNSRC
CLNACC	RCV000197297.1,