rs1057517021

Orientation

minus

Stabilized

minus

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

Make rs1057517021(-;-)

Make rs1057517021(-;A)

Reference

GRCh38.p7 38.3/150

Chromosome

19

Position

35845681

Gene

NPHS1

is a	snp
is	mentioned by
dbSNP	rs1057517021
dbSNP (classic)	rs1057517021
ClinGen	rs1057517021
ebi	rs1057517021
HLI	rs1057517021
Exac	rs1057517021
Gnomad	rs1057517021
Varsome	rs1057517021
LitVar	rs1057517021
Map	rs1057517021
PheGenI	rs1057517021
Biobank	rs1057517021
1000 genomes	rs1057517021
hgdp	rs1057517021
ensembl	rs1057517021
geneview	rs1057517021
scholar	rs1057517021
google	rs1057517021
pharmgkb	rs1057517021
gwascentral	rs1057517021
openSNP	rs1057517021
23andMe	rs1057517021
SNPshot	rs1057517021
SNPdbe	rs1057517021
MSV3d	rs1057517021
GWAS Ctlg	rs1057517021

Max Magnitude

0

ClinVar
Risk	rs1057517021(-;-)
Alt	rs1057517021(-;-)
Reference	Rs1057517021(A;A)
Significance	Probable-Pathogenic
Disease	Finnish congenital nephrotic syndrome
Variation	info
Gene	NPHS1
CLNDBN	Finnish congenital nephrotic syndrome
Reversed	1
HGVS	NC_000019.9:g.36336583delT
CLNSRC
CLNACC	RCV000408979.1,