rs863223856

Orientation

plus

Stabilized

plus

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

Make rs863223856(C;T)

Make rs863223856(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

3

Position

30671943

Gene

TGFBR2

is a	snp
is	mentioned by
dbSNP	rs863223856
dbSNP (classic)	rs863223856
ClinGen	rs863223856
ebi	rs863223856
HLI	rs863223856
Exac	rs863223856
Gnomad	rs863223856
Varsome	rs863223856
LitVar	rs863223856
Map	rs863223856
PheGenI	rs863223856
Biobank	rs863223856
1000 genomes	rs863223856
hgdp	rs863223856
ensembl	rs863223856
geneview	rs863223856
scholar	rs863223856
google	rs863223856
pharmgkb	rs863223856
gwascentral	rs863223856
openSNP	rs863223856
23andMe	rs863223856
SNPshot	rs863223856
SNPdbe	rs863223856
MSV3d	rs863223856
GWAS Ctlg	rs863223856

Max Magnitude

0

ClinVar
Risk	rs863223856(T;T)
Alt	rs863223856(T;T)
Reference	Rs863223856(C;C)
Significance	Pathogenic
Disease	not specified
Variation	info
Gene	TGFBR2
CLNDBN	not specified
Reversed	0
HGVS	NC_000003.11:g.30713435C>T
CLNSRC
CLNACC	RCV000198902.3,