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rs6970262

From SNPedia

Orientationplus
Stabilizedplus
Make rs6970262(A;A)
Make rs6970262(A;G)
Make rs6970262(G;G)
ReferenceGRCh38 38.1/142
Chromosome7
Position55192070
GeneEGFR
is asnp
is mentioned by
dbSNPrs6970262
dbSNP (old)rs6970262
ClinGenrs6970262
ebirs6970262
HLIrs6970262
Exacrs6970262
Varsomers6970262
Maprs6970262
PheGenIrs6970262
Biobankrs6970262
1000 genomesrs6970262
hgdprs6970262
ensemblrs6970262
gopubmedrs6970262
geneviewrs6970262
scholarrs6970262
googlers6970262
pharmgkbrs6970262
gwascentralrs6970262
openSNPrs6970262
23andMers6970262
23andMe allrs6970262
SNP Nexus

SNPshotrs6970262
SNPdbers6970262
MSV3drs6970262
GWAS Ctlgrs6970262
Max Magnitude
? (A;A) (A;G) (G;G) 28
[PMID 25511740OA-icon.png] Identification of epidermal growth factor receptor (EGFR) genetic variants that modify risk for head and neck squamous cell carcinoma