rs863223793

Orientation

plus

Stabilized

plus

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

Make rs863223793(G;T)

Make rs863223793(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

1

Position

218437363

Gene

TGFB2

is a	snp
is	mentioned by
dbSNP	rs863223793
dbSNP (classic)	rs863223793
ClinGen	rs863223793
ebi	rs863223793
HLI	rs863223793
Exac	rs863223793
Gnomad	rs863223793
Varsome	rs863223793
LitVar	rs863223793
Map	rs863223793
PheGenI	rs863223793
Biobank	rs863223793
1000 genomes	rs863223793
hgdp	rs863223793
ensembl	rs863223793
geneview	rs863223793
scholar	rs863223793
google	rs863223793
pharmgkb	rs863223793
gwascentral	rs863223793
openSNP	rs863223793
23andMe	rs863223793
SNPshot	rs863223793
SNPdbe	rs863223793
MSV3d	rs863223793
GWAS Ctlg	rs863223793

Max Magnitude

0

ClinVar
Risk	rs863223793(T;T)
Alt	rs863223793(T;T)
Reference	Rs863223793(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	TGFB2
CLNDBN	not provided
Reversed	0
HGVS	NC_000001.10:g.218610705G>T
CLNSRC
CLNACC	RCV000197949.1,