rs863223796

Orientation

plus

Stabilized

plus

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

Make rs863223796(-;A)

Make rs863223796(A;A)

Reference

GRCh38.p2 38.2/146

Chromosome

1

Position

218436036

Gene

TGFB2

is a	snp
is	mentioned by
dbSNP	rs863223796
dbSNP (classic)	rs863223796
ClinGen	rs863223796
ebi	rs863223796
HLI	rs863223796
Exac	rs863223796
Gnomad	rs863223796
Varsome	rs863223796
LitVar	rs863223796
Map	rs863223796
PheGenI	rs863223796
Biobank	rs863223796
1000 genomes	rs863223796
hgdp	rs863223796
ensembl	rs863223796
geneview	rs863223796
scholar	rs863223796
google	rs863223796
pharmgkb	rs863223796
gwascentral	rs863223796
openSNP	rs863223796
23andMe	rs863223796
SNPshot	rs863223796
SNPdbe	rs863223796
MSV3d	rs863223796
GWAS Ctlg	rs863223796

Max Magnitude

0

ClinVar
Risk	rs863223796(A;A)
Alt	rs863223796(A;A)
Reference	Rs863223796(-;-)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	TGFB2
CLNDBN	not provided
Reversed	0
HGVS	NC_000001.10:g.218609378dupA
CLNSRC
CLNACC	RCV000197799.1,