rs1060499703

Orientation

minus

Stabilized

minus

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

Make rs1060499703(A;A)

Make rs1060499703(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

1

Position

179559762

Gene

NPHS2

is a	snp
is	mentioned by
dbSNP	rs1060499703
dbSNP (classic)	rs1060499703
ClinGen	rs1060499703
ebi	rs1060499703
HLI	rs1060499703
Exac	rs1060499703
Gnomad	rs1060499703
Varsome	rs1060499703
LitVar	rs1060499703
Map	rs1060499703
PheGenI	rs1060499703
Biobank	rs1060499703
1000 genomes	rs1060499703
hgdp	rs1060499703
ensembl	rs1060499703
geneview	rs1060499703
scholar	rs1060499703
google	rs1060499703
pharmgkb	rs1060499703
gwascentral	rs1060499703
openSNP	rs1060499703
23andMe	rs1060499703
SNPshot	rs1060499703
SNPdbe	rs1060499703
MSV3d	rs1060499703
GWAS Ctlg	rs1060499703

Max Magnitude

0

ClinVar
Risk	rs1060499703(A;A)
Alt	rs1060499703(A;A)
Reference	Rs1060499703(G;G)
Significance	Pathogenic
Disease	Nephrotic syndrome
Variation	info
Gene	NPHS2
CLNDBN	Nephrotic syndrome, idiopathic, steroid-resistant
Reversed	1
HGVS	NC_000001.10:g.179528897C>T
CLNSRC
CLNACC	RCV000449520.1,