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rs17290699

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs17290699(A;C)
Make rs17290699(C;C)
ReferenceGRCh38 38.1/141
Chromosome7
Position55201204
GeneEGFR
is asnp
is mentioned by
dbSNPrs17290699
ebirs17290699
HLIrs17290699
Exacrs17290699
Varsomers17290699
Maprs17290699
PheGenIrs17290699
hapmaprs17290699
1000 genomesrs17290699
hgdprs17290699
ensemblrs17290699
gopubmedrs17290699
geneviewrs17290699
scholarrs17290699
googlers17290699
pharmgkbrs17290699
gwascentralrs17290699
openSNPrs17290699
23andMers17290699
23andMe allrs17290699
SNP Nexus

SNPshotrs17290699
SNPdbers17290699
MSV3drs17290699
GWAS Ctlgrs17290699
GMAF0.007805
Max Magnitude0
? (A;A) (A;C) (C;C) 28

[PMID 20049516] Investigating the Function of Three Non-Synonymous SNPs in EGFR Gene: Structural Modelling and Association With Breast Cancer


[PMID 17956637OA-icon.png] Polymorphisms in the epidermal growth factor receptor gene and the risk of primary lung cancer: a case-control study.


GET Evidence
EGFR-H988P
aa_change His988Pro
aa_change_short H988P
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.00957427
summary



ClinVar
Risk rs17290699(C,G;C,G)
Alt rs17290699(C,G;C,G)
Reference rs17290699(A;A)
Significance Untested
Disease not specified
Variation info
Gene EGFR
CLNDBN not specified
Reversed 0
HGVS NC_000007.13:g.55268897A>C
CLNSRC ClinVar
CLNACC RCV000120698.1,