rs1057521150

Orientation

plus

Stabilized

plus

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

Make rs1057521150(A;A)

Make rs1057521150(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

1

Position

218436111

Gene

TGFB2

is a	snp
is	mentioned by
dbSNP	rs1057521150
dbSNP (classic)	rs1057521150
ClinGen	rs1057521150
ebi	rs1057521150
HLI	rs1057521150
Exac	rs1057521150
Gnomad	rs1057521150
Varsome	rs1057521150
LitVar	rs1057521150
Map	rs1057521150
PheGenI	rs1057521150
Biobank	rs1057521150
1000 genomes	rs1057521150
hgdp	rs1057521150
ensembl	rs1057521150
geneview	rs1057521150
scholar	rs1057521150
google	rs1057521150
pharmgkb	rs1057521150
gwascentral	rs1057521150
openSNP	rs1057521150
23andMe	rs1057521150
SNPshot	rs1057521150
SNPdbe	rs1057521150
MSV3d	rs1057521150
GWAS Ctlg	rs1057521150

Max Magnitude

0

ClinVar
Risk	rs1057521150(A;A)
Alt	rs1057521150(A;A)
Reference	Rs1057521150(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	TGFB2
CLNDBN	not provided
Reversed	0
HGVS	NC_000001.10:g.218609453G>A
CLNSRC
CLNACC	RCV000418728.1,