rs74315347

Orientation

minus

Stabilized

minus

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

Make rs74315347(A;A)

Make rs74315347(A;G)

Reference

GRCh38 38.1/141

Chromosome

1

Position

179557227

Gene

NPHS2

is a	snp
is	mentioned by
dbSNP	rs74315347
dbSNP (classic)	rs74315347
ClinGen	rs74315347
ebi	rs74315347
HLI	rs74315347
Exac	rs74315347
Gnomad	rs74315347
Varsome	rs74315347
LitVar	rs74315347
Map	rs74315347
PheGenI	rs74315347
Biobank	rs74315347
1000 genomes	rs74315347
hgdp	rs74315347
ensembl	rs74315347
geneview	rs74315347
scholar	rs74315347
google	rs74315347
pharmgkb	rs74315347
gwascentral	rs74315347
openSNP	rs74315347
23andMe	rs74315347
SNPshot	rs74315347
SNPdbe	rs74315347
MSV3d	rs74315347
GWAS Ctlg	rs74315347

Max Magnitude

0

OMIM	604766
Desc
Variant	0009
Related	also

ClinVar
Risk	rs74315347(A;A)
Alt	rs74315347(A;A)
Reference	Rs74315347(G;G)
Significance	Other
Disease	Nephrotic syndrome
Variation	info
Gene	NPHS2
CLNDBN	Nephrotic syndrome, idiopathic, steroid-resistant
Reversed	1
HGVS	NC_000001.10:g.179526362C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000005699.4,