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rs1057520037

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057520037(C;C)
Make rs1057520037(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position55174782
GeneEGFR
is asnp
is mentioned by
dbSNPrs1057520037
dbSNP (old)rs1057520037
ClinGenrs1057520037
ebirs1057520037
HLIrs1057520037
Exacrs1057520037
Gnomadrs1057520037
Varsomers1057520037
Maprs1057520037
PheGenIrs1057520037
Biobankrs1057520037
1000 genomesrs1057520037
hgdprs1057520037
ensemblrs1057520037
gopubmedrs1057520037
geneviewrs1057520037
scholarrs1057520037
googlers1057520037
pharmgkbrs1057520037
gwascentralrs1057520037
openSNPrs1057520037
23andMers1057520037
23andMe allrs1057520037
SNPshotrs1057520037
SNPdbers1057520037
MSV3drs1057520037
GWAS Ctlgrs1057520037
Max Magnitude0
ClinVar
Risk rs1057520037(C;C)
Alt rs1057520037(C;C)
Reference Rs1057520037(G;G)
Significance Probable-Pathogenic
Disease Lung cancer
Variation info
Gene EGFR
CLNDBN Lung cancer
Reversed 0
HGVS NC_000007.13:g.55242475G>C
CLNSRC
CLNACC RCV000444877.1,