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rs139236063

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs139236063(G;T)
Make rs139236063(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position55165350
GeneEGFR
is asnp
is mentioned by
dbSNPrs139236063
dbSNP (old)rs139236063
ClinGenrs139236063
ebirs139236063
HLIrs139236063
Exacrs139236063
Gnomadrs139236063
Varsomers139236063
Maprs139236063
PheGenIrs139236063
Biobankrs139236063
1000 genomesrs139236063
hgdprs139236063
ensemblrs139236063
gopubmedrs139236063
geneviewrs139236063
scholarrs139236063
googlers139236063
pharmgkbrs139236063
gwascentralrs139236063
openSNPrs139236063
23andMers139236063
23andMe allrs139236063
SNP Nexus

SNPshotrs139236063
SNPdbers139236063
MSV3drs139236063
GWAS Ctlgrs139236063
Max Magnitude0
ClinVar
Risk rs139236063(C;C) rs139236063(T;T)
Alt rs139236063(C;C) rs139236063(T;T)
Reference Rs139236063(G;G)
Significance Probable-Pathogenic
Disease Neoplasm of brain Brainstem glioma Glioblastoma
Variation info
Gene EGFR
CLNDBN Neoplasm of brain Brainstem glioma Glioblastoma
Reversed 0
HGVS NC_000007.13:g.55233043G>C; NC_000007.13:g.55233043G>T
CLNSRC
CLNACC RCV000423114.1, RCV000429899.1, RCV000440786.1, RCV000418494.1, RCV000434448.1, RCV000436167.1,