rs1057516637

Orientation

minus

Stabilized

minus

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

Make rs1057516637(-;C)

Make rs1057516637(C;C)

Reference

GRCh38.p7 38.3/150

Chromosome

19

Position

35835755

Gene

NPHS1

is a	snp
is	mentioned by
dbSNP	rs1057516637
dbSNP (classic)	rs1057516637
ClinGen	rs1057516637
ebi	rs1057516637
HLI	rs1057516637
Exac	rs1057516637
Gnomad	rs1057516637
Varsome	rs1057516637
LitVar	rs1057516637
Map	rs1057516637
PheGenI	rs1057516637
Biobank	rs1057516637
1000 genomes	rs1057516637
hgdp	rs1057516637
ensembl	rs1057516637
geneview	rs1057516637
scholar	rs1057516637
google	rs1057516637
pharmgkb	rs1057516637
gwascentral	rs1057516637
openSNP	rs1057516637
23andMe	rs1057516637
SNPshot	rs1057516637
SNPdbe	rs1057516637
MSV3d	rs1057516637
GWAS Ctlg	rs1057516637

Max Magnitude

0

ClinVar
Risk	rs1057516637(C;C)
Alt	rs1057516637(C;C)
Reference	Rs1057516637(-;-)
Significance	Probable-Pathogenic
Disease	Finnish congenital nephrotic syndrome
Variation	info
Gene	NPHS1
CLNDBN	Finnish congenital nephrotic syndrome
Reversed	1
HGVS	NC_000019.9:g.36326658dupG
CLNSRC
CLNACC	RCV000409058.1,