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rs1057519887

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(GC;GC) 0 common in clinvar
Make rs1057519887(AA;AA)
Make rs1057519887(AA;GC)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position55154128
GeneEGFR
is asnp
is mentioned by
dbSNPrs1057519887
dbSNP (old)rs1057519887
ClinGenrs1057519887
ebirs1057519887
HLIrs1057519887
Exacrs1057519887
Gnomadrs1057519887
Varsomers1057519887
Maprs1057519887
PheGenIrs1057519887
Biobankrs1057519887
1000 genomesrs1057519887
hgdprs1057519887
ensemblrs1057519887
gopubmedrs1057519887
geneviewrs1057519887
scholarrs1057519887
googlers1057519887
pharmgkbrs1057519887
gwascentralrs1057519887
openSNPrs1057519887
23andMers1057519887
23andMe allrs1057519887
SNP Nexus

SNPshotrs1057519887
SNPdbers1057519887
MSV3drs1057519887
GWAS Ctlgrs1057519887
Max Magnitude0
ClinVar
Risk rs1057519887(AA;AA) rs1057519887(AT;AT)
Alt rs1057519887(AA;AA) rs1057519887(AT;AT)
Reference Rs1057519887(GC;GC)
Significance Probable-Pathogenic
Disease Glioblastoma Squamous cell carcinoma of the head and neck Neoplasm of brain
Variation info
Gene EGFR
CLNDBN Glioblastoma Squamous cell carcinoma of the head and neck Neoplasm of brain
Reversed 0
HGVS NC_000007.13:g.55221821_55221822delGCinsAA; NC_000007.13:g.55221821_55221822delGCinsAT
CLNSRC
CLNACC RCV000424975.1, RCV000437629.1, RCV000442544.1, RCV000417429.1, RCV000429429.1, RCV000435251.1,