rs863223843

Orientation

plus

Stabilized

plus

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

Make rs863223843(C;T)

Make rs863223843(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

3

Position

30672303

Gene

TGFBR2

is a	snp
is	mentioned by
dbSNP	rs863223843
dbSNP (classic)	rs863223843
ClinGen	rs863223843
ebi	rs863223843
HLI	rs863223843
Exac	rs863223843
Gnomad	rs863223843
Varsome	rs863223843
LitVar	rs863223843
Map	rs863223843
PheGenI	rs863223843
Biobank	rs863223843
1000 genomes	rs863223843
hgdp	rs863223843
ensembl	rs863223843
geneview	rs863223843
scholar	rs863223843
google	rs863223843
pharmgkb	rs863223843
gwascentral	rs863223843
openSNP	rs863223843
23andMe	rs863223843
SNPshot	rs863223843
SNPdbe	rs863223843
MSV3d	rs863223843
GWAS Ctlg	rs863223843

Max Magnitude

0

ClinVar
Risk	rs863223843(T;T)
Alt	rs863223843(T;T)
Reference	Rs863223843(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	TGFBR2
CLNDBN	not provided
Reversed	0
HGVS	NC_000003.11:g.30713795C>T
CLNSRC
CLNACC	RCV000196206.1,