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rs3203713

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs3203713(A;G)
Make rs3203713(G;G)
ReferenceGRCh38 38.1/142
Chromosome10
Position94327971
GenePLCE1
is asnp
is mentioned by
dbSNPrs3203713
dbSNP (classic)rs3203713
ClinGenrs3203713
ebirs3203713
HLIrs3203713
Exacrs3203713
Gnomadrs3203713
Varsomers3203713
LitVarrs3203713
Maprs3203713
PheGenIrs3203713
Biobankrs3203713
1000 genomesrs3203713
hgdprs3203713
ensemblrs3203713
geneviewrs3203713
scholarrs3203713
googlers3203713
pharmgkbrs3203713
gwascentralrs3203713
openSNPrs3203713
23andMers3203713
SNPshotrs3203713
SNPdbers3203713
MSV3drs3203713
GWAS Ctlgrs3203713
GMAF0.09642
Max Magnitude0

[PMID 21689432OA-icon.png] 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,