rs869312746

Orientation

minus

Stabilized

minus

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

Make rs869312746(C;T)

Make rs869312746(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

1

Position

179575750

Gene

NPHS2

is a	snp
is	mentioned by
dbSNP	rs869312746
dbSNP (classic)	rs869312746
ClinGen	rs869312746
ebi	rs869312746
HLI	rs869312746
Exac	rs869312746
Gnomad	rs869312746
Varsome	rs869312746
LitVar	rs869312746
Map	rs869312746
PheGenI	rs869312746
Biobank	rs869312746
1000 genomes	rs869312746
hgdp	rs869312746
ensembl	rs869312746
geneview	rs869312746
scholar	rs869312746
google	rs869312746
pharmgkb	rs869312746
gwascentral	rs869312746
openSNP	rs869312746
23andMe	rs869312746
SNPshot	rs869312746
SNPdbe	rs869312746
MSV3d	rs869312746
GWAS Ctlg	rs869312746

Max Magnitude

0

ClinVar
Risk	rs869312746(T;T)
Alt	rs869312746(T;T)
Reference	Rs869312746(C;C)
Significance	Pathogenic
Disease	Nephrotic syndrome
Variation	info
Gene	NPHS2
CLNDBN	Nephrotic syndrome, idiopathic, steroid-resistant
Reversed	1
HGVS	NC_000001.10:g.179544885G>A
CLNSRC
CLNACC	RCV000210047.1,