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rs1057519848

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TG;TG) 0 common in clinvar
Make rs1057519848(GT;GT)
Make rs1057519848(GT;TG)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position55191822
GeneEGFR
is asnp
is mentioned by
dbSNPrs1057519848
dbSNP (old)rs1057519848
ClinGenrs1057519848
ebirs1057519848
HLIrs1057519848
Exacrs1057519848
Gnomadrs1057519848
Varsomers1057519848
Maprs1057519848
PheGenIrs1057519848
Biobankrs1057519848
1000 genomesrs1057519848
hgdprs1057519848
ensemblrs1057519848
gopubmedrs1057519848
geneviewrs1057519848
scholarrs1057519848
googlers1057519848
pharmgkbrs1057519848
gwascentralrs1057519848
openSNPrs1057519848
23andMers1057519848
23andMe allrs1057519848
SNPshotrs1057519848
SNPdbers1057519848
MSV3drs1057519848
GWAS Ctlgrs1057519848
Max Magnitude0
ClinVar
Risk rs1057519848(GT;GT)
Alt rs1057519848(GT;GT)
Reference Rs1057519848(TG;TG)
Significance Probable-Pathogenic
Disease Non-small cell lung cancer
Variation info
Gene EGFR
CLNDBN Non-small cell lung cancer
Reversed 0
HGVS NC_000007.13:g.55259515_55259516delTGinsGT
CLNSRC
CLNACC RCV000425876.1,