rs74315342

Orientation

minus

Stabilized

minus

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

Make rs74315342(A;A)

Make rs74315342(A;G)

Reference

GRCh38 38.1/142

Chromosome

1

Position

179561327

Gene

NPHS2

is a	snp
is	mentioned by
dbSNP	rs74315342
dbSNP (classic)	rs74315342
ClinGen	rs74315342
ebi	rs74315342
HLI	rs74315342
Exac	rs74315342
Gnomad	rs74315342
Varsome	rs74315342
LitVar	rs74315342
Map	rs74315342
PheGenI	rs74315342
Biobank	rs74315342
1000 genomes	rs74315342
hgdp	rs74315342
ensembl	rs74315342
geneview	rs74315342
scholar	rs74315342
google	rs74315342
pharmgkb	rs74315342
gwascentral	rs74315342
openSNP	rs74315342
23andMe	rs74315342
SNPshot	rs74315342
SNPdbe	rs74315342
MSV3d	rs74315342
GWAS Ctlg	rs74315342

Max Magnitude

0

OMIM	604766
Desc
Variant	0001
Related	also

ClinVar
Risk	rs74315342(A;A)
Alt	rs74315342(A;A)
Reference	Rs74315342(G;G)
Significance	Other
Disease	Nephrotic syndrome Steroid-resistant nephrotic syndrome not provided
Variation	info
Gene	NPHS2
CLNDBN	Nephrotic syndrome, idiopathic, steroid-resistant Steroid-resistant nephrotic syndrome not provided
Reversed	1
HGVS	NC_000001.10:g.179530462C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000005691.3, RCV000282488.1, RCV000414576.1,