rs61747728

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common on affy axiom data

Make rs61747728(C;T)

Make rs61747728(T;T)

Reference

GRCh38 38.1/141

Chromosome

1

Position

179557079

Gene

NPHS2

is a	snp
is	mentioned by
dbSNP	rs61747728
dbSNP (classic)	rs61747728
ClinGen	rs61747728
ebi	rs61747728
HLI	rs61747728
Exac	rs61747728
Gnomad	rs61747728
Varsome	rs61747728
LitVar	rs61747728
Map	rs61747728
PheGenI	rs61747728
Biobank	rs61747728
1000 genomes	rs61747728
hgdp	rs61747728
ensembl	rs61747728
geneview	rs61747728
scholar	rs61747728
google	rs61747728
pharmgkb	rs61747728
gwascentral	rs61747728
openSNP	rs61747728
23andMe	rs61747728
SNPshot	rs61747728
SNPdbe	rs61747728
MSV3d	rs61747728
GWAS Ctlg	rs61747728

GMAF

0.02158

Max Magnitude

0

OMIM	604766
Desc
Variant	0011
Related	also

ClinVar
Risk	rs61747728(T;T)
Alt	rs61747728(T;T)
Reference	Rs61747728(C;C)
Significance	Other
Disease	Nephrotic syndrome Proteinuria
Variation	info
Gene	NPHS2
CLNDBN	Nephrotic syndrome, type 2, susceptibility to Proteinuria
Reversed	0
HGVS	NC_000001.10:g.179526214C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000005701.3, RCV000157404.2,