rs1057516395

Orientation

minus

Stabilized

minus

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

Make rs1057516395(-;-)

Make rs1057516395(-;C)

Reference

GRCh38.p7 38.3/150

Chromosome

1

Position

179564699

Gene

NPHS2

is a	snp
is	mentioned by
dbSNP	rs1057516395
dbSNP (classic)	rs1057516395
ClinGen	rs1057516395
ebi	rs1057516395
HLI	rs1057516395
Exac	rs1057516395
Gnomad	rs1057516395
Varsome	rs1057516395
LitVar	rs1057516395
Map	rs1057516395
PheGenI	rs1057516395
Biobank	rs1057516395
1000 genomes	rs1057516395
hgdp	rs1057516395
ensembl	rs1057516395
geneview	rs1057516395
scholar	rs1057516395
google	rs1057516395
pharmgkb	rs1057516395
gwascentral	rs1057516395
openSNP	rs1057516395
23andMe	rs1057516395
SNPshot	rs1057516395
SNPdbe	rs1057516395
MSV3d	rs1057516395
GWAS Ctlg	rs1057516395

Max Magnitude

0

ClinVar
Risk	rs1057516395(-;-)
Alt	rs1057516395(-;-)
Reference	Rs1057516395(C;C)
Significance	Probable-Pathogenic
Disease	Nephrotic syndrome
Variation	info
Gene	NPHS2
CLNDBN	Nephrotic syndrome, idiopathic, steroid-resistant
Reversed	1
HGVS	NC_000001.10:g.179533834delG
CLNSRC
CLNACC	RCV000412170.1,