rs1057518597

Orientation

plus

Stabilized

plus

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

Make rs1057518597(-;-)

Make rs1057518597(-;A)

Reference

GRCh38.p7 38.3/150

Chromosome

1

Position

218405241

Gene

TGFB2

is a	snp
is	mentioned by
dbSNP	rs1057518597
dbSNP (classic)	rs1057518597
ClinGen	rs1057518597
ebi	rs1057518597
HLI	rs1057518597
Exac	rs1057518597
Gnomad	rs1057518597
Varsome	rs1057518597
LitVar	rs1057518597
Map	rs1057518597
PheGenI	rs1057518597
Biobank	rs1057518597
1000 genomes	rs1057518597
hgdp	rs1057518597
ensembl	rs1057518597
geneview	rs1057518597
scholar	rs1057518597
google	rs1057518597
pharmgkb	rs1057518597
gwascentral	rs1057518597
openSNP	rs1057518597
23andMe	rs1057518597
SNPshot	rs1057518597
SNPdbe	rs1057518597
MSV3d	rs1057518597
GWAS Ctlg	rs1057518597

Max Magnitude

0

ClinVar
Risk	rs1057518597(-;-)
Alt	rs1057518597(-;-)
Reference	Rs1057518597(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	TGFB2
CLNDBN	not provided
Reversed	0
HGVS	NC_000001.10:g.218578583delA
CLNSRC
CLNACC	RCV000414052.1,