rs863223853

Orientation

plus

Stabilized

plus

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

Make rs863223853(G;T)

Make rs863223853(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

3

Position

30691421

Gene

TGFBR2

is a	snp
is	mentioned by
dbSNP	rs863223853
dbSNP (classic)	rs863223853
ClinGen	rs863223853
ebi	rs863223853
HLI	rs863223853
Exac	rs863223853
Gnomad	rs863223853
Varsome	rs863223853
LitVar	rs863223853
Map	rs863223853
PheGenI	rs863223853
Biobank	rs863223853
1000 genomes	rs863223853
hgdp	rs863223853
ensembl	rs863223853
geneview	rs863223853
scholar	rs863223853
google	rs863223853
pharmgkb	rs863223853
gwascentral	rs863223853
openSNP	rs863223853
23andMe	rs863223853
SNPshot	rs863223853
SNPdbe	rs863223853
MSV3d	rs863223853
GWAS Ctlg	rs863223853

Max Magnitude

0

ClinVar
Risk	rs863223853(T;T)
Alt	rs863223853(T;T)
Reference	Rs863223853(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	TGFBR2
CLNDBN	not provided
Reversed	0
HGVS	NC_000003.11:g.30732913G>T
CLNSRC	UniProtKB (protein)
CLNACC	RCV000195860.1,