rs1057516747

Orientation

minus

Stabilized

minus

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

Make rs1057516747(-;GGGCT)

Make rs1057516747(GGGCT;GGGCT)

Reference

GRCh38.p7 38.3/150

Chromosome

1

Position

179575722

Gene

NPHS2

is a	snp
is	mentioned by
dbSNP	rs1057516747
dbSNP (classic)	rs1057516747
ClinGen	rs1057516747
ebi	rs1057516747
HLI	rs1057516747
Exac	rs1057516747
Gnomad	rs1057516747
Varsome	rs1057516747
LitVar	rs1057516747
Map	rs1057516747
PheGenI	rs1057516747
Biobank	rs1057516747
1000 genomes	rs1057516747
hgdp	rs1057516747
ensembl	rs1057516747
geneview	rs1057516747
scholar	rs1057516747
google	rs1057516747
pharmgkb	rs1057516747
gwascentral	rs1057516747
openSNP	rs1057516747
23andMe	rs1057516747
SNPshot	rs1057516747
SNPdbe	rs1057516747
MSV3d	rs1057516747
GWAS Ctlg	rs1057516747

Max Magnitude

0

ClinVar
Risk	rs1057516747(GGGCT;GGGCT)
Alt	rs1057516747(GGGCT;GGGCT)
Reference	Rs1057516747(-;-)
Significance	Probable-Pathogenic
Disease	Nephrotic syndrome
Variation	info
Gene	NPHS2
CLNDBN	Nephrotic syndrome, idiopathic, steroid-resistant
Reversed	1
HGVS	NC_000001.10:g.179544858_179544862dupAGCCC
CLNSRC
CLNACC	RCV000411511.1,