rs3203713

plus

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

Make rs3203713(A;G)

Make rs3203713(G;G)

Reference

GRCh38 38.1/142

Chromosome

10

Position

94327971

Gene

PLCE1

is a	snp
is	mentioned by
dbSNP	rs3203713
dbSNP (classic)	rs3203713
ClinGen	rs3203713
ebi	rs3203713
HLI	rs3203713
Exac	rs3203713
Gnomad	rs3203713
Varsome	rs3203713
LitVar	rs3203713
Map	rs3203713
PheGenI	rs3203713
Biobank	rs3203713
1000 genomes	rs3203713
hgdp	rs3203713
ensembl	rs3203713
geneview	rs3203713
scholar	rs3203713
google	rs3203713
pharmgkb	rs3203713
gwascentral	rs3203713
openSNP	rs3203713
23andMe	rs3203713
SNPshot	rs3203713
SNPdbe	rs3203713
MSV3d	rs3203713
GWAS Ctlg	rs3203713

GMAF

0.09642

Max Magnitude

0

[PMID 21689432 ] Association between novel PLCE1 variants identified in published esophageal cancer genome-wide association studies and risk of squamous cell carcinoma of the head and neck

?

(A;A) (A;G) (G;G)

ClinVar
Risk	rs3203713(G;G)
Alt	rs3203713(G;G)
Reference	Rs3203713(A;A)
Significance	Probable-non-pathogenic
Disease	Nephrotic syndrome
Variation	info
Gene	PLCE1
CLNDBN	Nephrotic syndrome
Reversed	0
HGVS	NC_000010.10:g.96087728A>G
CLNSRC
CLNACC	RCV000292908.1,