Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs397514464
rs397514464
PDE4D
1 1.000 0.240 5 59193511 missense variant G/T snv 0.800 1.000 4 2012 2013
dbSNP: rs397514465
rs397514465
PDE4D
3 0.925 0.280 5 59193507 missense variant A/C;G snv 0.800 1.000 4 2012 2013
dbSNP: rs397514466
rs397514466
PDE4D
1 1.000 0.240 5 59215856 missense variant A/C snv 0.800 1.000 4 2012 2013
dbSNP: rs397514467
rs397514467
PDE4D
2 0.925 0.240 5 58976421 missense variant T/G snv 0.800 1.000 4 2012 2013
dbSNP: rs397514468
rs397514468
PDE4D
1 1.000 0.240 5 59193502 missense variant G/C snv 0.800 1.000 4 2012 2013
dbSNP: rs397514469
rs397514469
PDE4D
1 1.000 0.240 5 58975076 missense variant C/T snv 0.800 1.000 4 2012 2013
dbSNP: rs397515433
rs397515433
PDE4D
1 1.000 0.240 5 59038869 missense variant G/A snv 0.800 1.000 4 2012 2013
dbSNP: rs587777188
rs587777188
PDE4D
1 1.000 0.240 5 58975061 missense variant A/G snv 0.800 1.000 4 2012 2013
dbSNP: rs1554033934
rs1554033934
PDE4D
1 1.000 0.240 5 58976418 missense variant T/C snv 0.700 0
dbSNP: rs387906744
rs387906744
PDE4D
1 1.000 0.240 5 58975718 missense variant T/G snv 0.700 0