rs17417407

plus

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

Make rs17417407(G;T)

Make rs17417407(T;T)

Reference

GRCh38 38.1/142

Chromosome

10

Position

94171330

Gene

PLCE1

is a	snp
is	mentioned by
dbSNP	rs17417407
dbSNP (classic)	rs17417407
ClinGen	rs17417407
ebi	rs17417407
HLI	rs17417407
Exac	rs17417407
Gnomad	rs17417407
Varsome	rs17417407
LitVar	rs17417407
Map	rs17417407
PheGenI	rs17417407
Biobank	rs17417407
1000 genomes	rs17417407
hgdp	rs17417407
ensembl	rs17417407
geneview	rs17417407
scholar	rs17417407
google	rs17417407
pharmgkb	rs17417407
gwascentral	rs17417407
openSNP	rs17417407
23andMe	rs17417407
SNPshot	rs17417407
SNPdbe	rs17417407
MSV3d	rs17417407
GWAS Ctlg	rs17417407

GMAF

0.1644

Max Magnitude

0

?

(G;G) (G;T) (T;T)

28

[PMID 23688607] Novel functional variants locus in PLCE1 and susceptibility to esophageal squamous cell carcinoma: Based on published genome-wide association studies in a central Chinese population

[PMID 22865593 ] Distinct genetic association at the PLCE1 locus with oesophageal squamous cell carcinoma in the South African population.

ClinVar
Risk	rs17417407(A;A) rs17417407(T;T)
Alt	rs17417407(A;A) rs17417407(T;T)
Reference	Rs17417407(G;G)
Significance	Non-pathogenic
Disease	not specified Nephrotic syndrome
Variation	info
Gene	PLCE1
CLNDBN	not specified Nephrotic syndrome
Reversed	0
HGVS	NC_000010.10:g.95931087G>T
CLNSRC
CLNACC	RCV000242119.1, RCV000269488.1,