rs267606918

Orientation

minus

Stabilized

minus

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

Make rs267606918(A;A)

Make rs267606918(A;G)

Reference

GRCh38 38.1/141

Chromosome

19

Position

35842421

Gene

NPHS1

is a	snp
is	mentioned by
dbSNP	rs267606918
dbSNP (classic)	rs267606918
ClinGen	rs267606918
ebi	rs267606918
HLI	rs267606918
Exac	rs267606918
Gnomad	rs267606918
Varsome	rs267606918
LitVar	rs267606918
Map	rs267606918
PheGenI	rs267606918
Biobank	rs267606918
1000 genomes	rs267606918
hgdp	rs267606918
ensembl	rs267606918
geneview	rs267606918
scholar	rs267606918
google	rs267606918
pharmgkb	rs267606918
gwascentral	rs267606918
openSNP	rs267606918
23andMe	rs267606918
SNPshot	rs267606918
SNPdbe	rs267606918
MSV3d	rs267606918
GWAS Ctlg	rs267606918

Max Magnitude

0

ClinVar
Risk	rs267606918(A;A)
Alt	rs267606918(A;A)
Reference	Rs267606918(G;G)
Significance	Pathogenic
Disease	Finnish congenital nephrotic syndrome
Variation	info
Gene	NPHS1
CLNDBN	Finnish congenital nephrotic syndrome
Reversed	1
HGVS	NC_000019.9:g.36333323C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000007278.2,