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rs1057519829

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057519829(A;C)
Make rs1057519829(C;C)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position55154050
GeneEGFR
is asnp
is mentioned by
dbSNPrs1057519829
dbSNP (old)rs1057519829
ClinGenrs1057519829
ebirs1057519829
HLIrs1057519829
Exacrs1057519829
Gnomadrs1057519829
Varsomers1057519829
Maprs1057519829
PheGenIrs1057519829
Biobankrs1057519829
1000 genomesrs1057519829
hgdprs1057519829
ensemblrs1057519829
gopubmedrs1057519829
geneviewrs1057519829
scholarrs1057519829
googlers1057519829
pharmgkbrs1057519829
gwascentralrs1057519829
openSNPrs1057519829
23andMers1057519829
23andMe allrs1057519829
SNP Nexus

SNPshotrs1057519829
SNPdbers1057519829
MSV3drs1057519829
GWAS Ctlgrs1057519829
Max Magnitude0
ClinVar
Risk rs1057519829(C;C)
Alt rs1057519829(C;C)
Reference Rs1057519829(A;A)
Significance Probable-Pathogenic
Disease Neoplasm of brain
Variation info
Gene EGFR
CLNDBN Neoplasm of brain
Reversed 0
HGVS NC_000007.13:g.55221743A>C
CLNSRC
CLNACC RCV000444169.1,