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rs7799627

From SNPedia

Orientationplus
Stabilizedplus
Make rs7799627(A;A)
Make rs7799627(A;G)
Make rs7799627(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position55093463
GeneEGFR
is asnp
is mentioned by
dbSNPrs7799627
ebirs7799627
HLIrs7799627
Exacrs7799627
Varsomers7799627
Maprs7799627
PheGenIrs7799627
hapmaprs7799627
1000 genomesrs7799627
hgdprs7799627
ensemblrs7799627
gopubmedrs7799627
geneviewrs7799627
scholarrs7799627
googlers7799627
pharmgkbrs7799627
gwascentralrs7799627
openSNPrs7799627
23andMers7799627
23andMe allrs7799627
SNP Nexus

SNPshotrs7799627
SNPdbers7799627
MSV3drs7799627
GWAS Ctlgrs7799627
GMAF0.2328
Max Magnitude
? (A;A) (A;G) (G;G) 28
[PMID 23251617OA-icon.png] Genetic variations in the transforming growth factor Beta pathway as predictors of bladder cancer risk