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rs121913230

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121913230(A;A)
Make rs121913230(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position55181437
GeneEGFR, EGFR-AS1
is asnp
is mentioned by
dbSNPrs121913230
dbSNP (old)rs121913230
ClinGenrs121913230
ebirs121913230
HLIrs121913230
Exacrs121913230
Gnomadrs121913230
Varsomers121913230
Maprs121913230
PheGenIrs121913230
Biobankrs121913230
1000 genomesrs121913230
hgdprs121913230
ensemblrs121913230
gopubmedrs121913230
geneviewrs121913230
scholarrs121913230
googlers121913230
pharmgkbrs121913230
gwascentralrs121913230
openSNPrs121913230
23andMers121913230
23andMe allrs121913230
SNP Nexus

SNPshotrs121913230
SNPdbers121913230
MSV3drs121913230
GWAS Ctlgrs121913230
Max Magnitude0
ClinVar
Risk rs121913230(A;A)
Alt rs121913230(A;A)
Reference Rs121913230(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.55249130G>A
CLNSRC
CLNACC RCV000444211.1,