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rs146795390

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs146795390(A;A)
Make rs146795390(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position55191776
GeneEGFR
is asnp
is mentioned by
dbSNPrs146795390
dbSNP (old)rs146795390
ClinGenrs146795390
ebirs146795390
HLIrs146795390
Exacrs146795390
Gnomadrs146795390
Varsomers146795390
LitVarrs146795390
Maprs146795390
PheGenIrs146795390
Biobankrs146795390
1000 genomesrs146795390
hgdprs146795390
ensemblrs146795390
gopubmedrs146795390
geneviewrs146795390
scholarrs146795390
googlers146795390
pharmgkbrs146795390
gwascentralrs146795390
openSNPrs146795390
23andMers146795390
23andMe allrs146795390
SNPshotrs146795390
SNPdbers146795390
MSV3drs146795390
GWAS Ctlgrs146795390
Max Magnitude0
ClinVar
Risk rs146795390(A;A)
Alt rs146795390(A;A)
Reference Rs146795390(G;G)
Significance Probable-Pathogenic
Disease Head and Neck Neoplasms
Variation info
Gene EGFR
CLNDBN Head and Neck Neoplasms
Reversed 0
HGVS NC_000007.13:g.55259469G>A
CLNSRC
CLNACC RCV000426205.1,