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: rs142480126
rs142480126
APOE
1 19 44907825 missense variant G/A snv 8.0E-06 0.020 1.000 2 2009 2009
dbSNP: rs1001030257
rs1001030257
PDE4D
1 5 58988559 missense variant T/C snv 2.0E-05 2.1E-05 0.010 1.000 1 2009 2009
dbSNP: rs10068737
rs10068737 		1 5 118700852 intergenic variant T/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs1009840
rs1009840
SGK1 ; LOC107986646
1 6 134225547 intron variant G/A snv 0.53 0.700 1.000 1 2011 2011
dbSNP: rs11078903
rs11078903
CDK12
2 17 39475671 intron variant G/A;C;T snv 0.700 1.000 1 2012 2012
dbSNP: rs1156619081
rs1156619081
UCP3
1 11 74005787 missense variant T/C snv 4.0E-06 0.010 1.000 1 2009 2009
dbSNP: rs11575542
rs11575542
DDC ; FIGNL1
1 7 50463289 missense variant C/T snv 2.3E-02 5.5E-02 0.010 1.000 1 2019 2019
dbSNP: rs1168357
rs1168357
GRIP1
1 12 66356099 intron variant T/C snv 0.50 0.700 1.000 1 2012 2012
dbSNP: rs12124078
rs12124078
DNAJC16
3 1 15543404 intron variant A/G snv 0.32 0.700 1.000 1 2012 2012
dbSNP: rs1232013698
rs1232013698
TNF
1 6 31577208 missense variant G/T snv 4.1E-06 0.010 1.000 1 2009 2009
dbSNP: rs12575381
rs12575381 		1 11 135033566 regulatory region variant G/A snv 0.16 0.700 1.000 1 2011 2011
dbSNP: rs12721226
rs12721226
AGTR1
1 3 148741522 missense variant G/A snv 6.3E-04 1.6E-04 0.010 1.000 1 2009 2009
dbSNP: rs1290773788
rs1290773788
PDE4D
1 5 58989799 missense variant C/T snv 0.010 1.000 1 2009 2009
dbSNP: rs1300938986
rs1300938986
PTGS1
1 9 122392516 missense variant C/T snv 4.0E-06 0.010 1.000 1 2009 2009
dbSNP: rs1318525693
rs1318525693
UCP3
1 11 74006370 missense variant C/G;T snv 0.010 1.000 1 2009 2009
dbSNP: rs1419367513
rs1419367513
ACAT2 ; SOD2 ; SOD2-OT1
1 6 159762678 non coding transcript exon variant G/A snv 0.010 1.000 1 2009 2009
dbSNP: rs1423621991
rs1423621991
MMP1 ; WTAPP1
1 11 102796745 missense variant C/T snv 0.010 1.000 1 2009 2009
dbSNP: rs1455341183
rs1455341183
PDE4D
1 5 59038945 missense variant C/T snv 0.010 1.000 1 2009 2009
dbSNP: rs1500896
rs1500896
C8orf37-AS1
1 8 95474454 intron variant G/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs1564858
rs1564858
TNFRSF11B
1 8 118932927 splice region variant G/A snv 0.11 9.9E-02 0.010 1.000 1 2019 2019
dbSNP: rs17384213
rs17384213
DDAH1
1 1 85418938 intron variant G/A snv 0.13 0.010 1.000 1 2010 2010
dbSNP: rs188780113
rs188780113
ATG2A
1 11 64911072 missense variant G/A snv 5.7E-04 1.5E-04 0.010 1.000 1 2017 2017
dbSNP: rs2030712
rs2030712
HIPK2 ; LOC105375530
1 7 139610185 intron variant C/A;T snv 0.010 1.000 1 2013 2013
dbSNP: rs2074379
rs2074379
ALPK1
3 1.000 4 112431743 missense variant G/A snv 0.62 0.65 0.010 1.000 1 2015 2015
dbSNP: rs2074380
rs2074380
ALPK1
2 4 112432155 missense variant G/A;T snv 8.5E-03; 2.4E-05 0.010 1.000 1 2013 2013