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rs121913431

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121913431(A;A)
Make rs121913431(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position55181438
GeneEGFR, EGFR-AS1
is asnp
is mentioned by
dbSNPrs121913431
dbSNP (old)rs121913431
ClinGenrs121913431
ebirs121913431
HLIrs121913431
Exacrs121913431
Gnomadrs121913431
Varsomers121913431
Maprs121913431
PheGenIrs121913431
Biobankrs121913431
1000 genomesrs121913431
hgdprs121913431
ensemblrs121913431
gopubmedrs121913431
geneviewrs121913431
scholarrs121913431
googlers121913431
pharmgkbrs121913431
gwascentralrs121913431
openSNPrs121913431
23andMers121913431
23andMe allrs121913431
SNPshotrs121913431
SNPdbers121913431
MSV3drs121913431
GWAS Ctlgrs121913431
Max Magnitude0
ClinVar
Risk rs121913431(A;A)
Alt rs121913431(A;A)
Reference Rs121913431(G;G)
Significance Probable-Pathogenic
Disease Squamous cell carcinoma
Variation info
Gene EGFR EGFR-AS1
CLNDBN Squamous cell carcinoma
Reversed 0
HGVS NC_000007.13:g.55249131G>A
CLNSRC
CLNACC RCV000425650.1,