rs1057517413

Orientation

minus

Stabilized

minus

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

Make rs1057517413(C;C)

Make rs1057517413(C;G)

Reference

GRCh38.p7 38.3/150

Chromosome

19

Position

35848795

Gene

NPHS1

is a	snp
is	mentioned by
dbSNP	rs1057517413
dbSNP (classic)	rs1057517413
ClinGen	rs1057517413
ebi	rs1057517413
HLI	rs1057517413
Exac	rs1057517413
Gnomad	rs1057517413
Varsome	rs1057517413
LitVar	rs1057517413
Map	rs1057517413
PheGenI	rs1057517413
Biobank	rs1057517413
1000 genomes	rs1057517413
hgdp	rs1057517413
ensembl	rs1057517413
geneview	rs1057517413
scholar	rs1057517413
google	rs1057517413
pharmgkb	rs1057517413
gwascentral	rs1057517413
openSNP	rs1057517413
23andMe	rs1057517413
SNPshot	rs1057517413
SNPdbe	rs1057517413
MSV3d	rs1057517413
GWAS Ctlg	rs1057517413

Max Magnitude

0

ClinVar
Risk	rs1057517413(C;C)
Alt	rs1057517413(C;C)
Reference	Rs1057517413(G;G)
Significance	Probable-Pathogenic
Disease	Finnish congenital nephrotic syndrome
Variation	info
Gene	NPHS1
CLNDBN	Finnish congenital nephrotic syndrome
Reversed	1
HGVS	NC_000019.9:g.36339697C>G
CLNSRC
CLNACC	RCV000410344.1,