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rs11569017

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs11569017(A;T)
Make rs11569017(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position109980955
GeneEGF
is asnp
is mentioned by
dbSNPrs11569017
dbSNP (old)rs11569017
ClinGenrs11569017
ebirs11569017
HLIrs11569017
Exacrs11569017
Gnomadrs11569017
Varsomers11569017
Maprs11569017
PheGenIrs11569017
Biobankrs11569017
1000 genomesrs11569017
hgdprs11569017
ensemblrs11569017
gopubmedrs11569017
geneviewrs11569017
scholarrs11569017
googlers11569017
pharmgkbrs11569017
gwascentralrs11569017
openSNPrs11569017
23andMers11569017
23andMe allrs11569017
SNP Nexus

SNPshotrs11569017
SNPdbers11569017
MSV3drs11569017
GWAS Ctlgrs11569017
GMAF0.09183
Max Magnitude0
? (A;A) (A;T) (T;T) 28
[PMID 22504456] A study of the functional significance of epidermal growth factor in major depressive disorder


[PMID 23790025OA-icon.png] Association of epidermal growth factor and epidermal growth factor receptor polymorphisms with the risk of hepatitis B virus-related hepatocellular carcinoma in the population of North China.


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


ClinVar
Risk rs11569017(T;T)
Alt rs11569017(T;T)
Reference Rs11569017(A;A)
Significance Probable-non-pathogenic
Disease Renal Hypomagnesemia
Variation info
Gene EGF
CLNDBN Renal Hypomagnesemia, Recessive
Reversed 0
HGVS NC_000004.11:g.110902111A>T
CLNSRC
CLNACC RCV000297814.1,