rs1057516880

Orientation

minus

Stabilized

minus

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

Make rs1057516880(-;TA)

Make rs1057516880(TA;TA)

Reference

GRCh38.p7 38.3/150

Chromosome

1

Position

179575769

Gene

NPHS2

is a	snp
is	mentioned by
dbSNP	rs1057516880
dbSNP (classic)	rs1057516880
ClinGen	rs1057516880
ebi	rs1057516880
HLI	rs1057516880
Exac	rs1057516880
Gnomad	rs1057516880
Varsome	rs1057516880
LitVar	rs1057516880
Map	rs1057516880
PheGenI	rs1057516880
Biobank	rs1057516880
1000 genomes	rs1057516880
hgdp	rs1057516880
ensembl	rs1057516880
geneview	rs1057516880
scholar	rs1057516880
google	rs1057516880
pharmgkb	rs1057516880
gwascentral	rs1057516880
openSNP	rs1057516880
23andMe	rs1057516880
SNPshot	rs1057516880
SNPdbe	rs1057516880
MSV3d	rs1057516880
GWAS Ctlg	rs1057516880

Max Magnitude

0

ClinVar
Risk	rs1057516880(TA;TA)
Alt	rs1057516880(TA;TA)
Reference	Rs1057516880(-;-)
Significance	Probable-Pathogenic
Disease	Nephrotic syndrome
Variation	info
Gene	NPHS2
CLNDBN	Nephrotic syndrome, idiopathic, steroid-resistant
Reversed	1
HGVS	NC_000001.10:g.179544904_179544905insTA
CLNSRC
CLNACC	RCV000410922.1,