rs1057517054

Orientation

minus

Stabilized

minus

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

Make rs1057517054(C;C)

Make rs1057517054(C;T)

Reference

GRCh38.p7 38.3/150

Chromosome

19

Position

35851260

Gene	KIRREL2, NPHS1

is a	snp
is	mentioned by
dbSNP	rs1057517054
dbSNP (classic)	rs1057517054
ClinGen	rs1057517054
ebi	rs1057517054
HLI	rs1057517054
Exac	rs1057517054
Gnomad	rs1057517054
Varsome	rs1057517054
LitVar	rs1057517054
Map	rs1057517054
PheGenI	rs1057517054
Biobank	rs1057517054
1000 genomes	rs1057517054
hgdp	rs1057517054
ensembl	rs1057517054
geneview	rs1057517054
scholar	rs1057517054
google	rs1057517054
pharmgkb	rs1057517054
gwascentral	rs1057517054
openSNP	rs1057517054
23andMe	rs1057517054
SNPshot	rs1057517054
SNPdbe	rs1057517054
MSV3d	rs1057517054
GWAS Ctlg	rs1057517054

Max Magnitude

0

ClinVar
Risk	rs1057517054(C;C)
Alt	rs1057517054(C;C)
Reference	Rs1057517054(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.36342162A>G
CLNSRC
CLNACC	RCV000410346.1,