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rs4698803

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs4698803(A;T)
Make rs4698803(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position109993271
GeneEGF
is asnp
is mentioned by
dbSNPrs4698803
dbSNP (classic)rs4698803
ClinGenrs4698803
ebirs4698803
HLIrs4698803
Exacrs4698803
Gnomadrs4698803
Varsomers4698803
LitVarrs4698803
Maprs4698803
PheGenIrs4698803
Biobankrs4698803
1000 genomesrs4698803
hgdprs4698803
ensemblrs4698803
geneviewrs4698803
scholarrs4698803
googlers4698803
pharmgkbrs4698803
gwascentralrs4698803
openSNPrs4698803
23andMers4698803
SNPshotrs4698803
SNPdbers4698803
MSV3drs4698803
GWAS Ctlgrs4698803
Max Magnitude0
? (A;A) (A;T) (T;T) 28


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


ClinVar
Risk rs4698803(T;T)
Alt rs4698803(T;T)
Reference Rs4698803(A;A)
Significance Non-pathogenic
Disease Renal Hypomagnesemia
Variation info
Gene EGF
CLNDBN Renal Hypomagnesemia, Recessive
Reversed 0
HGVS NC_000004.11:g.110914427A>T
CLNSRC
CLNACC RCV000323639.1,