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rs121913432

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121913432(A;G)
Make rs121913432(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position55181327
GeneEGFR, EGFR-AS1
is asnp
is mentioned by
dbSNPrs121913432
dbSNP (old)rs121913432
ClinGenrs121913432
ebirs121913432
HLIrs121913432
Exacrs121913432
Gnomadrs121913432
Varsomers121913432
Maprs121913432
PheGenIrs121913432
Biobankrs121913432
1000 genomesrs121913432
hgdprs121913432
ensemblrs121913432
gopubmedrs121913432
geneviewrs121913432
scholarrs121913432
googlers121913432
pharmgkbrs121913432
gwascentralrs121913432
openSNPrs121913432
23andMers121913432
23andMe allrs121913432
SNPshotrs121913432
SNPdbers121913432
MSV3drs121913432
GWAS Ctlgrs121913432
Max Magnitude0
ClinVar
Risk rs121913432(G;G)
Alt rs121913432(G;G)
Reference Rs121913432(A;A)
Significance Probable-Pathogenic
Disease Non-small cell lung cancer
Variation info
Gene EGFR EGFR-AS1
CLNDBN Non-small cell lung cancer
Reversed 0
HGVS NC_000007.13:g.55249020A>G
CLNSRC
CLNACC RCV000420488.1,