rs387906578

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(-;T)	3	Carrier for a renal tubular dysgenesis mutation
(T;T)	0	common in clinvar

Make rs387906578(-;-)

Reference

GRCh38 38.1/141

Chromosome

1

Position

230703309

Gene

AGT

is a	snp
is	mentioned by
dbSNP	rs387906578
dbSNP (classic)	rs387906578
ClinGen	rs387906578
ebi	rs387906578
HLI	rs387906578
Exac	rs387906578
Gnomad	rs387906578
Varsome	rs387906578
LitVar	rs387906578
Map	rs387906578
PheGenI	rs387906578
Biobank	rs387906578
1000 genomes	rs387906578
hgdp	rs387906578
ensembl	rs387906578
geneview	rs387906578
scholar	rs387906578
google	rs387906578
pharmgkb	rs387906578
gwascentral	rs387906578
openSNP	rs387906578
23andMe	rs387906578
SNPshot	rs387906578
SNPdbe	rs387906578
MSV3d	rs387906578
GWAS Ctlg	rs387906578

Max Magnitude

3

see OMIM 106150.0005

ClinVar
Risk	rs387906578(-;-)
Alt	rs387906578(-;-)
Reference	Rs387906578(T;T)
Significance	Pathogenic
Disease	Renal dysplasia
Variation	info
Gene	AGT
CLNDBN	Renal dysplasia
Reversed	1
HGVS	NC_000001.10:g.230839055delA
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000019698.29,