rs775170915

Orientation

plus

Stabilized

plus

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

Make rs775170915(-;-)

Make rs775170915(-;A)

Reference

GRCh38.p2 38.2/144

Chromosome

1

Position

179551377

Gene	AXDND1, NPHS2

is a	snp
is	mentioned by
dbSNP	rs775170915
dbSNP (classic)	rs775170915
ClinGen	rs775170915
ebi	rs775170915
HLI	rs775170915
Exac	rs775170915
Gnomad	rs775170915
Varsome	rs775170915
LitVar	rs775170915
Map	rs775170915
PheGenI	rs775170915
Biobank	rs775170915
1000 genomes	rs775170915
hgdp	rs775170915
ensembl	rs775170915
geneview	rs775170915
scholar	rs775170915
google	rs775170915
pharmgkb	rs775170915
gwascentral	rs775170915
openSNP	rs775170915
23andMe	rs775170915
SNPshot	rs775170915
SNPdbe	rs775170915
MSV3d	rs775170915
GWAS Ctlg	rs775170915

Max Magnitude

0

ClinVar
Risk	rs775170915(-;-)
Alt	rs775170915(-;-)
Reference	Rs775170915(A;A)
Significance	Probable-Pathogenic
Disease	Nephrotic syndrome
Variation	info
Gene	NPHS2 AXDND1
CLNDBN	Nephrotic syndrome, idiopathic, steroid-resistant
Reversed	0
HGVS	NC_000001.10:g.179520512delA
CLNSRC	Counsyl
CLNACC	RCV000169369.1,