rs12406197

Orientation

plus

Stabilized

plus

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

Make rs12406197(A;A)

Make rs12406197(A;C)

Reference

GRCh38.p2 38.2/147

Chromosome

1

Position

179575915

Gene

NPHS2

is a	snp
is	mentioned by
dbSNP	rs12406197
dbSNP (classic)	rs12406197
ClinGen	rs12406197
ebi	rs12406197
HLI	rs12406197
Exac	rs12406197
Gnomad	rs12406197
Varsome	rs12406197
LitVar	rs12406197
Map	rs12406197
PheGenI	rs12406197
Biobank	rs12406197
1000 genomes	rs12406197
hgdp	rs12406197
ensembl	rs12406197
geneview	rs12406197
scholar	rs12406197
google	rs12406197
pharmgkb	rs12406197
gwascentral	rs12406197
openSNP	rs12406197
23andMe	rs12406197
SNPshot	rs12406197
SNPdbe	rs12406197
MSV3d	rs12406197
GWAS Ctlg	rs12406197

Max Magnitude

0

ClinVar: Likely benign

ClinVar
Risk	rs12406197(A;A)
Alt	rs12406197(A;A)
Reference	Rs12406197(C;C)
Significance	Non-pathogenic
Disease	Nephrotic syndrome Steroid-resistant nephrotic syndrome
Variation	info
Gene	NPHS2
CLNDBN	Nephrotic syndrome, idiopathic, steroid-resistant Steroid-resistant nephrotic syndrome
Reversed	0
HGVS	NC_000001.10:g.179545050C>A
CLNSRC
CLNACC	RCV000210779.1, RCV000210804.1, RCV000358624.1,