rs763818901

Orientation

plus

Stabilized

plus

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

Make rs763818901(A;A)

Make rs763818901(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

1

Position

179551361

Gene	AXDND1, NPHS2

is a	snp
is	mentioned by
dbSNP	rs763818901
dbSNP (classic)	rs763818901
ClinGen	rs763818901
ebi	rs763818901
HLI	rs763818901
Exac	rs763818901
Gnomad	rs763818901
Varsome	rs763818901
LitVar	rs763818901
Map	rs763818901
PheGenI	rs763818901
Biobank	rs763818901
1000 genomes	rs763818901
hgdp	rs763818901
ensembl	rs763818901
geneview	rs763818901
scholar	rs763818901
google	rs763818901
pharmgkb	rs763818901
gwascentral	rs763818901
openSNP	rs763818901
23andMe	rs763818901
SNPshot	rs763818901
SNPdbe	rs763818901
MSV3d	rs763818901
GWAS Ctlg	rs763818901

Max Magnitude

0

ClinVar
Risk	rs763818901(A;A)
Alt	rs763818901(A;A)
Reference	Rs763818901(G;G)
Significance	Probable-Pathogenic
Disease	Nephrotic syndrome
Variation	info
Gene	NPHS2 AXDND1
CLNDBN	Nephrotic syndrome, idiopathic, steroid-resistant
Reversed	0
HGVS	NC_000001.10:g.179520496G>A
CLNSRC
CLNACC	RCV000412425.1,