rs1057517275

Orientation

minus

Stabilized

minus

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

Make rs1057517275(-;-)

Make rs1057517275(-;G)

Reference

GRCh38.p7 38.3/150

Chromosome

19

Position

35850377

Gene	KIRREL2, NPHS1

is a	snp
is	mentioned by
dbSNP	rs1057517275
dbSNP (classic)	rs1057517275
ClinGen	rs1057517275
ebi	rs1057517275
HLI	rs1057517275
Exac	rs1057517275
Gnomad	rs1057517275
Varsome	rs1057517275
LitVar	rs1057517275
Map	rs1057517275
PheGenI	rs1057517275
Biobank	rs1057517275
1000 genomes	rs1057517275
hgdp	rs1057517275
ensembl	rs1057517275
geneview	rs1057517275
scholar	rs1057517275
google	rs1057517275
pharmgkb	rs1057517275
gwascentral	rs1057517275
openSNP	rs1057517275
23andMe	rs1057517275
SNPshot	rs1057517275
SNPdbe	rs1057517275
MSV3d	rs1057517275
GWAS Ctlg	rs1057517275

Max Magnitude

0

ClinVar
Risk	rs1057517275(-;-)
Alt	rs1057517275(-;-)
Reference	Rs1057517275(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.36341279delC
CLNSRC
CLNACC	RCV000408986.1,