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rs1057519794

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057519794(A;A)
Make rs1057519794(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position55173927
GeneEGFR
is asnp
is mentioned by
dbSNPrs1057519794
dbSNP (old)rs1057519794
ClinGenrs1057519794
ebirs1057519794
HLIrs1057519794
Exacrs1057519794
Gnomadrs1057519794
Varsomers1057519794
Maprs1057519794
PheGenIrs1057519794
Biobankrs1057519794
1000 genomesrs1057519794
hgdprs1057519794
ensemblrs1057519794
gopubmedrs1057519794
geneviewrs1057519794
scholarrs1057519794
googlers1057519794
pharmgkbrs1057519794
gwascentralrs1057519794
openSNPrs1057519794
23andMers1057519794
23andMe allrs1057519794
SNP Nexus

SNPshotrs1057519794
SNPdbers1057519794
MSV3drs1057519794
GWAS Ctlgrs1057519794
Max Magnitude0
ClinVar
Risk rs1057519794(A;A)
Alt rs1057519794(A;A)
Reference Rs1057519794(G;G)
Significance Probable-Pathogenic
Disease Endometrial Endometrioid Adenocarcinoma
Variation info
Gene EGFR
CLNDBN Endometrial Endometrioid Adenocarcinoma, Variant with Squamous Differentiation
Reversed 0
HGVS NC_000007.13:g.55241620G>A
CLNSRC
CLNACC RCV000438760.1,