rs386833877

minus

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

Make rs386833877(-;A)

Make rs386833877(A;A)

Reference

GRCh38 38.1/141

Chromosome

19

Position

35848275

Gene

NPHS1

is a	snp
is	mentioned by
dbSNP	rs386833877
dbSNP (classic)	rs386833877
ClinGen	rs386833877
ebi	rs386833877
HLI	rs386833877
Exac	rs386833877
Gnomad	rs386833877
Varsome	rs386833877
LitVar	rs386833877
Map	rs386833877
PheGenI	rs386833877
Biobank	rs386833877
1000 genomes	rs386833877
hgdp	rs386833877
ensembl	rs386833877
geneview	rs386833877
scholar	rs386833877
google	rs386833877
pharmgkb	rs386833877
gwascentral	rs386833877
openSNP	rs386833877
23andMe	rs386833877
SNPshot	rs386833877
SNPdbe	rs386833877
MSV3d	rs386833877
GWAS Ctlg	rs386833877

Max Magnitude

0

ClinVar
Risk	rs386833877(A;A)
Alt	rs386833877(A;A)
Reference	Rs386833877(-;-)
Significance	Probable-Pathogenic
Disease	Finnish congenital nephrotic syndrome
Variation	info
Gene	NPHS1
CLNDBN	Finnish congenital nephrotic syndrome
Reversed	1
HGVS	NC_000019.9:g.36339178dupT
CLNSRC	ClinVar
CLNACC	RCV000049848.1,

[PMID 11854170] Genotype/phenotype correlations of NPHS1 and NPHS2 mutations in nephrotic syndrome advocate a functional inter-relationship in glomerular filtration.