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rs149840192

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs149840192(C;T)
Make rs149840192(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position55154129
GeneEGFR
is asnp
is mentioned by
dbSNPrs149840192
dbSNP (old)rs149840192
ClinGenrs149840192
ebirs149840192
HLIrs149840192
Exacrs149840192
Gnomadrs149840192
Varsomers149840192
Maprs149840192
PheGenIrs149840192
Biobankrs149840192
1000 genomesrs149840192
hgdprs149840192
ensemblrs149840192
gopubmedrs149840192
geneviewrs149840192
scholarrs149840192
googlers149840192
pharmgkbrs149840192
gwascentralrs149840192
openSNPrs149840192
23andMers149840192
23andMe allrs149840192
SNPshotrs149840192
SNPdbers149840192
MSV3drs149840192
GWAS Ctlgrs149840192
Max Magnitude0
ClinVar
Risk rs149840192(A;A) rs149840192(T;T)
Alt rs149840192(A;A) rs149840192(T;T)
Reference Rs149840192(C;C)
Significance Probable-Pathogenic
Disease Neoplasm of brain Glioblastoma Squamous cell carcinoma of the head and neck
Variation info
Gene EGFR
CLNDBN Neoplasm of brain Glioblastoma Squamous cell carcinoma of the head and neck
Reversed 0
HGVS NC_000007.13:g.55221822C>A; NC_000007.13:g.55221822C>T
CLNSRC
CLNACC RCV000427425.1, RCV000434840.1, RCV000443311.1, RCV000423404.1, RCV000423749.1, RCV000439402.1,