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rs1057519760

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057519760(A;G)
Make rs1057519760(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position55160314
GeneEGFR
is asnp
is mentioned by
dbSNPrs1057519760
dbSNP (old)rs1057519760
ClinGenrs1057519760
ebirs1057519760
HLIrs1057519760
Exacrs1057519760
Gnomadrs1057519760
Varsomers1057519760
LitVarrs1057519760
Maprs1057519760
PheGenIrs1057519760
Biobankrs1057519760
1000 genomesrs1057519760
hgdprs1057519760
ensemblrs1057519760
gopubmedrs1057519760
geneviewrs1057519760
scholarrs1057519760
googlers1057519760
pharmgkbrs1057519760
gwascentralrs1057519760
openSNPrs1057519760
23andMers1057519760
23andMe allrs1057519760
SNPshotrs1057519760
SNPdbers1057519760
MSV3drs1057519760
GWAS Ctlgrs1057519760
Max Magnitude0
ClinVar
Risk rs1057519760(G;G)
Alt rs1057519760(G;G)
Reference Rs1057519760(A;A)
Significance Probable-Pathogenic
Disease Colorectal Neoplasms
Variation info
Gene EGFR
CLNDBN Colorectal Neoplasms
Reversed 0
HGVS NC_000007.13:g.55228007A>G
CLNSRC
CLNACC RCV000429440.1,