rs876657369

Orientation

plus

Stabilized

plus

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

Make rs876657369(-;-)

Make rs876657369(-;G)

Reference

GRCh38.p2 38.2/147

Chromosome

10

Position

94032192

Gene

PLCE1

is a	snp
is	mentioned by
dbSNP	rs876657369
dbSNP (classic)	rs876657369
ClinGen	rs876657369
ebi	rs876657369
HLI	rs876657369
Exac	rs876657369
Gnomad	rs876657369
Varsome	rs876657369
LitVar	rs876657369
Map	rs876657369
PheGenI	rs876657369
Biobank	rs876657369
1000 genomes	rs876657369
hgdp	rs876657369
ensembl	rs876657369
geneview	rs876657369
scholar	rs876657369
google	rs876657369
pharmgkb	rs876657369
gwascentral	rs876657369
openSNP	rs876657369
23andMe	rs876657369
SNPshot	rs876657369
SNPdbe	rs876657369
MSV3d	rs876657369
GWAS Ctlg	rs876657369

Max Magnitude

0

ClinVar
Risk	rs876657369(-;-)
Alt	rs876657369(-;-)
Reference	Rs876657369(G;G)
Significance	Pathogenic
Disease	Nephrotic syndrome
Variation	info
Gene	PLCE1
CLNDBN	Nephrotic syndrome, type 3
Reversed	0
HGVS	NC_000010.10:g.95791949delG
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000002435.3,