rs863223842

Orientation

plus

Stabilized

plus

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

Make rs863223842(A;G)

Make rs863223842(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

3

Position

30672268

Gene

TGFBR2

is a	snp
is	mentioned by
dbSNP	rs863223842
dbSNP (classic)	rs863223842
ClinGen	rs863223842
ebi	rs863223842
HLI	rs863223842
Exac	rs863223842
Gnomad	rs863223842
Varsome	rs863223842
LitVar	rs863223842
Map	rs863223842
PheGenI	rs863223842
Biobank	rs863223842
1000 genomes	rs863223842
hgdp	rs863223842
ensembl	rs863223842
geneview	rs863223842
scholar	rs863223842
google	rs863223842
pharmgkb	rs863223842
gwascentral	rs863223842
openSNP	rs863223842
23andMe	rs863223842
SNPshot	rs863223842
SNPdbe	rs863223842
MSV3d	rs863223842
GWAS Ctlg	rs863223842

Max Magnitude

0

ClinVar
Risk	rs863223842(G;G)
Alt	rs863223842(G;G)
Reference	Rs863223842(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	TGFBR2
CLNDBN	not provided
Reversed	0
HGVS	NC_000003.11:g.30713760A>G
CLNSRC
CLNACC	RCV000200101.1,