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rs1057519830

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057519830(C;T)
Make rs1057519830(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position55163737
GeneEGFR
is asnp
is mentioned by
dbSNPrs1057519830
dbSNP (old)rs1057519830
ClinGenrs1057519830
ebirs1057519830
HLIrs1057519830
Exacrs1057519830
Gnomadrs1057519830
Varsomers1057519830
Maprs1057519830
PheGenIrs1057519830
Biobankrs1057519830
1000 genomesrs1057519830
hgdprs1057519830
ensemblrs1057519830
gopubmedrs1057519830
geneviewrs1057519830
scholarrs1057519830
googlers1057519830
pharmgkbrs1057519830
gwascentralrs1057519830
openSNPrs1057519830
23andMers1057519830
23andMe allrs1057519830
SNPshotrs1057519830
SNPdbers1057519830
MSV3drs1057519830
GWAS Ctlgrs1057519830
Max Magnitude0
ClinVar
Risk rs1057519830(T;T)
Alt rs1057519830(T;T)
Reference Rs1057519830(C;C)
Significance Probable-Pathogenic
Disease Head and Neck Neoplasms
Variation info
Gene EGFR
CLNDBN Head and Neck Neoplasms
Reversed 0
HGVS NC_000007.13:g.55231430C>T
CLNSRC
CLNACC RCV000443890.1,