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rs1057519828

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057519828(A;A)
Make rs1057519828(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position55143387
GeneEGFR
is asnp
is mentioned by
dbSNPrs1057519828
dbSNP (old)rs1057519828
ClinGenrs1057519828
ebirs1057519828
HLIrs1057519828
Exacrs1057519828
Gnomadrs1057519828
Varsomers1057519828
Maprs1057519828
PheGenIrs1057519828
Biobankrs1057519828
1000 genomesrs1057519828
hgdprs1057519828
ensemblrs1057519828
gopubmedrs1057519828
geneviewrs1057519828
scholarrs1057519828
googlers1057519828
pharmgkbrs1057519828
gwascentralrs1057519828
openSNPrs1057519828
23andMers1057519828
23andMe allrs1057519828
SNPshotrs1057519828
SNPdbers1057519828
MSV3drs1057519828
GWAS Ctlgrs1057519828
Max Magnitude0
ClinVar
Risk rs1057519828(A;A)
Alt rs1057519828(A;A)
Reference Rs1057519828(G;G)
Significance Probable-Pathogenic
Disease Neoplasm of brain
Variation info
Gene EGFR
CLNDBN Neoplasm of brain
Reversed 0
HGVS NC_000007.13:g.55211080G>A
CLNSRC
CLNACC RCV000432019.1,