rs863223795

Orientation

plus

Stabilized

plus

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

Make rs863223795(-;T)

Make rs863223795(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

1

Position

218434338

Gene

TGFB2

is a	snp
is	mentioned by
dbSNP	rs863223795
dbSNP (classic)	rs863223795
ClinGen	rs863223795
ebi	rs863223795
HLI	rs863223795
Exac	rs863223795
Gnomad	rs863223795
Varsome	rs863223795
LitVar	rs863223795
Map	rs863223795
PheGenI	rs863223795
Biobank	rs863223795
1000 genomes	rs863223795
hgdp	rs863223795
ensembl	rs863223795
geneview	rs863223795
scholar	rs863223795
google	rs863223795
pharmgkb	rs863223795
gwascentral	rs863223795
openSNP	rs863223795
23andMe	rs863223795
SNPshot	rs863223795
SNPdbe	rs863223795
MSV3d	rs863223795
GWAS Ctlg	rs863223795

Max Magnitude

0

ClinVar
Risk	rs863223795(T;T)
Alt	rs863223795(T;T)
Reference	Rs863223795(-;-)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	TGFB2
CLNDBN	not provided
Reversed	0
HGVS	NC_000001.10:g.218607680_218607681insT
CLNSRC
CLNACC	RCV000195595.1,