rs1057518029

Orientation

plus

Stabilized

plus

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

Make rs1057518029(A;G)

Make rs1057518029(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

1

Position

218434336

Gene

TGFB2

is a	snp
is	mentioned by
dbSNP	rs1057518029
dbSNP (classic)	rs1057518029
ClinGen	rs1057518029
ebi	rs1057518029
HLI	rs1057518029
Exac	rs1057518029
Gnomad	rs1057518029
Varsome	rs1057518029
LitVar	rs1057518029
Map	rs1057518029
PheGenI	rs1057518029
Biobank	rs1057518029
1000 genomes	rs1057518029
hgdp	rs1057518029
ensembl	rs1057518029
geneview	rs1057518029
scholar	rs1057518029
google	rs1057518029
pharmgkb	rs1057518029
gwascentral	rs1057518029
openSNP	rs1057518029
23andMe	rs1057518029
SNPshot	rs1057518029
SNPdbe	rs1057518029
MSV3d	rs1057518029
GWAS Ctlg	rs1057518029

Max Magnitude

0

ClinVar
Risk	rs1057518029(G;G)
Alt	rs1057518029(G;G)
Reference	Rs1057518029(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	TGFB2
CLNDBN	not provided
Reversed	0
HGVS	NC_000001.10:g.218607678A>G
CLNSRC
CLNACC	RCV000413467.1,