rs863223850

Orientation

plus

Stabilized

plus

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

Make rs863223850(C;T)

Make rs863223850(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

3

Position

30674129

Gene

TGFBR2

is a	snp
is	mentioned by
dbSNP	rs863223850
dbSNP (classic)	rs863223850
ClinGen	rs863223850
ebi	rs863223850
HLI	rs863223850
Exac	rs863223850
Gnomad	rs863223850
Varsome	rs863223850
LitVar	rs863223850
Map	rs863223850
PheGenI	rs863223850
Biobank	rs863223850
1000 genomes	rs863223850
hgdp	rs863223850
ensembl	rs863223850
geneview	rs863223850
scholar	rs863223850
google	rs863223850
pharmgkb	rs863223850
gwascentral	rs863223850
openSNP	rs863223850
23andMe	rs863223850
SNPshot	rs863223850
SNPdbe	rs863223850
MSV3d	rs863223850
GWAS Ctlg	rs863223850

Max Magnitude

0

ClinVar
Risk	rs863223850(T;T)
Alt	rs863223850(T;T)
Reference	Rs863223850(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	TGFBR2
CLNDBN	not provided
Reversed	0
HGVS	NC_000003.11:g.30715621C>T
CLNSRC
CLNACC	RCV000195460.1,