rs869025495

Orientation

minus

Stabilized

minus

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

Make rs869025495(C;T)

Make rs869025495(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

1

Position

179564715

Gene

NPHS2

is a	snp
is	mentioned by
dbSNP	rs869025495
dbSNP (classic)	rs869025495
ClinGen	rs869025495
ebi	rs869025495
HLI	rs869025495
Exac	rs869025495
Gnomad	rs869025495
Varsome	rs869025495
LitVar	rs869025495
Map	rs869025495
PheGenI	rs869025495
Biobank	rs869025495
1000 genomes	rs869025495
hgdp	rs869025495
ensembl	rs869025495
geneview	rs869025495
scholar	rs869025495
google	rs869025495
pharmgkb	rs869025495
gwascentral	rs869025495
openSNP	rs869025495
23andMe	rs869025495
SNPshot	rs869025495
SNPdbe	rs869025495
MSV3d	rs869025495
GWAS Ctlg	rs869025495

Max Magnitude

0

ClinVar
Risk	rs869025495(T;T)
Alt	rs869025495(T;T)
Reference	Rs869025495(C;C)
Significance	Pathogenic
Disease	Proteinuria
Variation	info
Gene	NPHS2
CLNDBN	Proteinuria
Reversed	1
HGVS	NC_000001.10:g.179533850G>A
CLNSRC
CLNACC	RCV000208227.1,