rs1057524810

Orientation

plus

Stabilized

plus

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

Make rs1057524810(A;A)

Make rs1057524810(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

3

Position

30691505

Gene

TGFBR2

is a	snp
is	mentioned by
dbSNP	rs1057524810
dbSNP (classic)	rs1057524810
ClinGen	rs1057524810
ebi	rs1057524810
HLI	rs1057524810
Exac	rs1057524810
Gnomad	rs1057524810
Varsome	rs1057524810
LitVar	rs1057524810
Map	rs1057524810
PheGenI	rs1057524810
Biobank	rs1057524810
1000 genomes	rs1057524810
hgdp	rs1057524810
ensembl	rs1057524810
geneview	rs1057524810
scholar	rs1057524810
google	rs1057524810
pharmgkb	rs1057524810
gwascentral	rs1057524810
openSNP	rs1057524810
23andMe	rs1057524810
SNPshot	rs1057524810
SNPdbe	rs1057524810
MSV3d	rs1057524810
GWAS Ctlg	rs1057524810

Max Magnitude

0

ClinVar
Risk	rs1057524810(A;A)
Alt	rs1057524810(A;A)
Reference	Rs1057524810(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	TGFBR2
CLNDBN	not provided
Reversed	0
HGVS	NC_000003.11:g.30732997G>A
CLNSRC
CLNACC	RCV000429672.1,