rs150855173

Orientation

plus

Stabilized

plus

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

Make rs150855173(A;A)

Make rs150855173(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

19

Position

35831092

Gene

NPHS1

is a	snp
is	mentioned by
dbSNP	rs150855173
dbSNP (classic)	rs150855173
ClinGen	rs150855173
ebi	rs150855173
HLI	rs150855173
Exac	rs150855173
Gnomad	rs150855173
Varsome	rs150855173
LitVar	rs150855173
Map	rs150855173
PheGenI	rs150855173
Biobank	rs150855173
1000 genomes	rs150855173
hgdp	rs150855173
ensembl	rs150855173
geneview	rs150855173
scholar	rs150855173
google	rs150855173
pharmgkb	rs150855173
gwascentral	rs150855173
openSNP	rs150855173
23andMe	rs150855173
SNPshot	rs150855173
SNPdbe	rs150855173
MSV3d	rs150855173
GWAS Ctlg	rs150855173

Max Magnitude

0

ClinVar
Risk	rs150855173(A;A)
Alt	rs150855173(A;A)
Reference	Rs150855173(G;G)
Significance	Probable-Pathogenic
Disease	Finnish congenital nephrotic syndrome
Variation	info
Gene	NPHS1
CLNDBN	Finnish congenital nephrotic syndrome
Reversed	0
HGVS	NC_000019.9:g.36321994G>A
CLNSRC
CLNACC	RCV000169477.1,