rs1057516942

Orientation

minus

Stabilized

minus

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

Make rs1057516942(-;-)

Make rs1057516942(-;T)

Reference

GRCh38.p7 38.3/150

Chromosome

19

Position

35851557

Gene	KIRREL2, NPHS1

is a	snp
is	mentioned by
dbSNP	rs1057516942
dbSNP (classic)	rs1057516942
ClinGen	rs1057516942
ebi	rs1057516942
HLI	rs1057516942
Exac	rs1057516942
Gnomad	rs1057516942
Varsome	rs1057516942
LitVar	rs1057516942
Map	rs1057516942
PheGenI	rs1057516942
Biobank	rs1057516942
1000 genomes	rs1057516942
hgdp	rs1057516942
ensembl	rs1057516942
geneview	rs1057516942
scholar	rs1057516942
google	rs1057516942
pharmgkb	rs1057516942
gwascentral	rs1057516942
openSNP	rs1057516942
23andMe	rs1057516942
SNPshot	rs1057516942
SNPdbe	rs1057516942
MSV3d	rs1057516942
GWAS Ctlg	rs1057516942

Max Magnitude

0

ClinVar
Risk	rs1057516942(-;-)
Alt	rs1057516942(-;-)
Reference	Rs1057516942(T;T)
Significance	Probable-Pathogenic
Disease	Finnish congenital nephrotic syndrome
Variation	info
Gene	NPHS1
CLNDBN	Finnish congenital nephrotic syndrome
Reversed	1
HGVS	NC_000019.9:g.36342459delA
CLNSRC
CLNACC	RCV000409163.1,