rs267606954

Orientation

plus

Stabilized

plus

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

Make rs267606954(C;T)

Make rs267606954(T;T)

Reference

GRCh38 38.1/141

Chromosome

10

Position

94032007

Gene

PLCE1

is a	snp
is	mentioned by
dbSNP	rs267606954
dbSNP (classic)	rs267606954
ClinGen	rs267606954
ebi	rs267606954
HLI	rs267606954
Exac	rs267606954
Gnomad	rs267606954
Varsome	rs267606954
LitVar	rs267606954
Map	rs267606954
PheGenI	rs267606954
Biobank	rs267606954
1000 genomes	rs267606954
hgdp	rs267606954
ensembl	rs267606954
geneview	rs267606954
scholar	rs267606954
google	rs267606954
pharmgkb	rs267606954
gwascentral	rs267606954
openSNP	rs267606954
23andMe	rs267606954
SNPshot	rs267606954
SNPdbe	rs267606954
MSV3d	rs267606954
GWAS Ctlg	rs267606954

Max Magnitude

0

ClinVar
Risk	rs267606954(T;T)
Alt	rs267606954(T;T)
Reference	Rs267606954(C;C)
Significance	Pathogenic
Disease	Nephrotic syndrome
Variation	info
Gene	PLCE1
CLNDBN	Nephrotic syndrome, type 3
Reversed	0
HGVS	NC_000010.10:g.95791764C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000002443.3,