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rs2237051

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs2237051(A;A)
Make rs2237051(A;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position109980042
GeneEGF
is asnp
is mentioned by
dbSNPrs2237051
dbSNP (classic)rs2237051
ClinGenrs2237051
ebirs2237051
HLIrs2237051
Exacrs2237051
Gnomadrs2237051
Varsomers2237051
LitVarrs2237051
Maprs2237051
PheGenIrs2237051
Biobankrs2237051
1000 genomesrs2237051
hgdprs2237051
ensemblrs2237051
geneviewrs2237051
scholarrs2237051
googlers2237051
pharmgkbrs2237051
gwascentralrs2237051
openSNPrs2237051
23andMers2237051
SNPshotrs2237051
SNPdbers2237051
MSV3drs2237051
GWAS Ctlgrs2237051
Max Magnitude0
? (A;A) (A;G) (G;G) 28


[PMID 24754849] Polymorphism in the epidermal growth factor gene is associated with pre-eclampsia and low birthweight


[PMID 24945674OA-icon.png] Genetic variants of EGF and VEGF predict prognosis of patients with advanced esophageal squamous cell carcinoma


ClinVar
Risk rs2237051(A;A)
Alt rs2237051(A;A)
Reference Rs2237051(G;G)
Significance Non-pathogenic
Disease Renal Hypomagnesemia
Variation info
Gene EGF
CLNDBN Renal Hypomagnesemia, Recessive
Reversed 0
HGVS NC_000004.11:g.110901198G>A
CLNSRC
CLNACC RCV000261366.1,



[PMID 31833563] A novel multi-locus genetic risk score identifies patients with higher risk of generalized aggressive periodontitis.


[PMID 31906817OA-icon.png] Association between epidermal growth factor (EGF) and EGF receptor gene polymorphisms and end-stage renal disease and acute renal allograft rejection in a Korean population.