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rs1057519888

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057519888(A;G)
Make rs1057519888(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position55143386
GeneEGFR
is asnp
is mentioned by
dbSNPrs1057519888
dbSNP (old)rs1057519888
ClinGenrs1057519888
ebirs1057519888
HLIrs1057519888
Exacrs1057519888
Gnomadrs1057519888
Varsomers1057519888
LitVarrs1057519888
Maprs1057519888
PheGenIrs1057519888
Biobankrs1057519888
1000 genomesrs1057519888
hgdprs1057519888
ensemblrs1057519888
gopubmedrs1057519888
geneviewrs1057519888
scholarrs1057519888
googlers1057519888
pharmgkbrs1057519888
gwascentralrs1057519888
openSNPrs1057519888
23andMers1057519888
23andMe allrs1057519888
SNPshotrs1057519888
SNPdbers1057519888
MSV3drs1057519888
GWAS Ctlgrs1057519888
Max Magnitude0
ClinVar
Risk rs1057519888(G;G)
Alt rs1057519888(G;G)
Reference Rs1057519888(A;A)
Significance Probable-Pathogenic
Disease Glioblastoma Neoplasm of brain Brainstem glioma
Variation info
Gene EGFR
CLNDBN Glioblastoma Neoplasm of brain Brainstem glioma
Reversed 0
HGVS NC_000007.13:g.55211079A>G
CLNSRC
CLNACC RCV000424206.1, RCV000434481.1, RCV000440142.1,