rs1057516776

Orientation

minus

Stabilized

minus

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

Make rs1057516776(A;A)

Make rs1057516776(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

19

Position

35848147

Gene

NPHS1

is a	snp
is	mentioned by
dbSNP	rs1057516776
dbSNP (classic)	rs1057516776
ClinGen	rs1057516776
ebi	rs1057516776
HLI	rs1057516776
Exac	rs1057516776
Gnomad	rs1057516776
Varsome	rs1057516776
LitVar	rs1057516776
Map	rs1057516776
PheGenI	rs1057516776
Biobank	rs1057516776
1000 genomes	rs1057516776
hgdp	rs1057516776
ensembl	rs1057516776
geneview	rs1057516776
scholar	rs1057516776
google	rs1057516776
pharmgkb	rs1057516776
gwascentral	rs1057516776
openSNP	rs1057516776
23andMe	rs1057516776
SNPshot	rs1057516776
SNPdbe	rs1057516776
MSV3d	rs1057516776
GWAS Ctlg	rs1057516776

Max Magnitude

0

ClinVar
Risk	rs1057516776(A;A)
Alt	rs1057516776(A;A)
Reference	Rs1057516776(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.36339049C>T
CLNSRC
CLNACC	RCV000412259.1,