rs1057516680

Orientation

minus

Stabilized

minus

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

Make rs1057516680(A;A)

Make rs1057516680(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

1

Position

179575862

Gene

NPHS2

is a	snp
is	mentioned by
dbSNP	rs1057516680
dbSNP (classic)	rs1057516680
ClinGen	rs1057516680
ebi	rs1057516680
HLI	rs1057516680
Exac	rs1057516680
Gnomad	rs1057516680
Varsome	rs1057516680
LitVar	rs1057516680
Map	rs1057516680
PheGenI	rs1057516680
Biobank	rs1057516680
1000 genomes	rs1057516680
hgdp	rs1057516680
ensembl	rs1057516680
geneview	rs1057516680
scholar	rs1057516680
google	rs1057516680
pharmgkb	rs1057516680
gwascentral	rs1057516680
openSNP	rs1057516680
23andMe	rs1057516680
SNPshot	rs1057516680
SNPdbe	rs1057516680
MSV3d	rs1057516680
GWAS Ctlg	rs1057516680

Max Magnitude

0

ClinVar
Risk	rs1057516680(A;A)
Alt	rs1057516680(A;A)
Reference	Rs1057516680(G;G)
Significance	Probable-Pathogenic
Disease	Nephrotic syndrome
Variation	info
Gene	NPHS2
CLNDBN	Nephrotic syndrome, idiopathic, steroid-resistant
Reversed	1
HGVS	NC_000001.10:g.179544997C>T
CLNSRC
CLNACC	RCV000409834.1,