rs1057517022

Orientation

minus

Stabilized

minus

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

Make rs1057517022(-;-)

Make rs1057517022(-;C)

Reference

GRCh38.p7 38.3/150

Chromosome

19

Position

35844419

Gene

NPHS1

is a	snp
is	mentioned by
dbSNP	rs1057517022
dbSNP (classic)	rs1057517022
ClinGen	rs1057517022
ebi	rs1057517022
HLI	rs1057517022
Exac	rs1057517022
Gnomad	rs1057517022
Varsome	rs1057517022
LitVar	rs1057517022
Map	rs1057517022
PheGenI	rs1057517022
Biobank	rs1057517022
1000 genomes	rs1057517022
hgdp	rs1057517022
ensembl	rs1057517022
geneview	rs1057517022
scholar	rs1057517022
google	rs1057517022
pharmgkb	rs1057517022
gwascentral	rs1057517022
openSNP	rs1057517022
23andMe	rs1057517022
SNPshot	rs1057517022
SNPdbe	rs1057517022
MSV3d	rs1057517022
GWAS Ctlg	rs1057517022

Max Magnitude

0

ClinVar
Risk	rs1057517022(-;-)
Alt	rs1057517022(-;-)
Reference	Rs1057517022(C;C)
Significance	Probable-Pathogenic
Disease	Finnish congenital nephrotic syndrome
Variation	info
Gene	NPHS1
CLNDBN	Finnish congenital nephrotic syndrome
Reversed	1
HGVS	NC_000019.9:g.36335321delG
CLNSRC
CLNACC	RCV000410557.1,