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rs1057520731

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057520731(G;G)
Make rs1057520731(G;T)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position59038899
GenePDE4D
is asnp
is mentioned by
dbSNPrs1057520731
dbSNP (old)rs1057520731
ClinGenrs1057520731
ebirs1057520731
HLIrs1057520731
Exacrs1057520731
Gnomadrs1057520731
Varsomers1057520731
LitVarrs1057520731
Maprs1057520731
PheGenIrs1057520731
Biobankrs1057520731
1000 genomesrs1057520731
hgdprs1057520731
ensemblrs1057520731
gopubmedrs1057520731
geneviewrs1057520731
scholarrs1057520731
googlers1057520731
pharmgkbrs1057520731
gwascentralrs1057520731
openSNPrs1057520731
23andMers1057520731
23andMe allrs1057520731
SNPshotrs1057520731
SNPdbers1057520731
MSV3drs1057520731
GWAS Ctlgrs1057520731
Max Magnitude0
ClinVar
Risk rs1057520731(G;G)
Alt rs1057520731(G;G)
Reference Rs1057520731(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene PDE4D
CLNDBN not provided
Reversed 1
HGVS NC_000005.9:g.58334726A>C
CLNSRC
CLNACC RCV000425291.1,