rs778055996

Orientation

plus

Stabilized

plus

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

Make rs778055996(A;A)

Make rs778055996(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

1

Position

179557122

Gene

NPHS2

is a	snp
is	mentioned by
dbSNP	rs778055996
dbSNP (classic)	rs778055996
ClinGen	rs778055996
ebi	rs778055996
HLI	rs778055996
Exac	rs778055996
Gnomad	rs778055996
Varsome	rs778055996
LitVar	rs778055996
Map	rs778055996
PheGenI	rs778055996
Biobank	rs778055996
1000 genomes	rs778055996
hgdp	rs778055996
ensembl	rs778055996
geneview	rs778055996
scholar	rs778055996
google	rs778055996
pharmgkb	rs778055996
gwascentral	rs778055996
openSNP	rs778055996
23andMe	rs778055996
SNPshot	rs778055996
SNPdbe	rs778055996
MSV3d	rs778055996
GWAS Ctlg	rs778055996

Max Magnitude

0

ClinVar
Risk	rs778055996(A;A) rs778055996(C;C)
Alt	rs778055996(A;A) rs778055996(C;C)
Reference	Rs778055996(G;G)
Significance	Probable-Pathogenic
Disease	Nephrotic syndrome
Variation	info
Gene	NPHS2
CLNDBN	Nephrotic syndrome, idiopathic, steroid-resistant
Reversed	0
HGVS	NC_000001.10:g.179526257G>A
CLNSRC
CLNACC	RCV000409295.1,