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rs1057515420

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome7
Position100819874
GeneEPHB4
is asnp
is mentioned by
dbSNPrs1057515420
dbSNP (old)rs1057515420
ClinGenrs1057515420
ebirs1057515420
HLIrs1057515420
Exacrs1057515420
Gnomadrs1057515420
Varsomers1057515420
Maprs1057515420
PheGenIrs1057515420
Biobankrs1057515420
1000 genomesrs1057515420
hgdprs1057515420
ensemblrs1057515420
gopubmedrs1057515420
geneviewrs1057515420
scholarrs1057515420
googlers1057515420
pharmgkbrs1057515420
gwascentralrs1057515420
openSNPrs1057515420
23andMers1057515420
23andMe allrs1057515420
SNPshotrs1057515420
SNPdbers1057515420
MSV3drs1057515420
GWAS Ctlgrs1057515420
Max Magnitude0
ClinVar
Risk rs1057515420(T;T)
Alt rs1057515420(T;T)
Reference Rs1057515420(C;C)
Significance Probable-Pathogenic
Disease Tetralogy of Fallot
Variation info
Gene EPHB4
CLNDBN Tetralogy of Fallot
Reversed 1
HGVS NC_000007.13:g.100417496G>A
CLNSRC
CLNACC RCV000408650.1,