rs267606955

Orientation

plus

Stabilized

plus

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

Make rs267606955(C;T)

Make rs267606955(T;T)

Reference

GRCh38 38.1/141

Chromosome

10

Position

94259072

Gene

PLCE1

is a	snp
is	mentioned by
dbSNP	rs267606955
dbSNP (classic)	rs267606955
ClinGen	rs267606955
ebi	rs267606955
HLI	rs267606955
Exac	rs267606955
Gnomad	rs267606955
Varsome	rs267606955
LitVar	rs267606955
Map	rs267606955
PheGenI	rs267606955
Biobank	rs267606955
1000 genomes	rs267606955
hgdp	rs267606955
ensembl	rs267606955
geneview	rs267606955
scholar	rs267606955
google	rs267606955
pharmgkb	rs267606955
gwascentral	rs267606955
openSNP	rs267606955
23andMe	rs267606955
SNPshot	rs267606955
SNPdbe	rs267606955
MSV3d	rs267606955
GWAS Ctlg	rs267606955

Max Magnitude

0

ClinVar
Risk	rs267606955(A;A) rs267606955(T;T)
Alt	rs267606955(A;A) rs267606955(T;T)
Reference	Rs267606955(C;C)
Significance	Pathogenic
Disease	Nephrotic syndrome
Variation	info
Gene	PLCE1
CLNDBN	Nephrotic syndrome, type 3
Reversed	0
HGVS	NC_000010.10:g.96018829C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000002444.3,