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: rs121434325
rs121434325
ERCC8
1 1.000 0.160 5 60904794 missense variant G/A snv 8.0E-06 7.1E-06 0.800 1.000 3 2004 2010
dbSNP: rs121434326
rs121434326
ERCC8
1 1.000 0.160 5 60902446 missense variant C/G snv 6.4E-05 0.710 1.000 3 2004 2010
dbSNP: rs281875222
rs281875222
ERCC8
1 1.000 0.160 5 60904795 missense variant C/T snv 7.1E-06 0.700 1.000 3 2004 2010
dbSNP: rs281875223
rs281875223
ERCC8
1 1.000 0.160 5 60902477 missense variant C/A;G snv 0.700 1.000 3 2004 2010
dbSNP: rs281875224
rs281875224
ERCC8
1 1.000 0.160 5 60902454 missense variant A/G snv 0.700 1.000 3 2004 2010
dbSNP: rs281875225
rs281875225
ERCC8
1 1.000 0.160 5 60898322 missense variant T/C;G snv 8.0E-06; 4.0E-06 0.700 1.000 3 2004 2010
dbSNP: rs121434324
rs121434324
ERCC8 ; NDUFAF2
1 1.000 0.160 5 60944972 stop gained C/A snv 7.6E-05 4.9E-05 0.710 1.000 2 2004 2010
dbSNP: rs201464610
rs201464610
ERCC8
1 1.000 0.160 5 60899728 splice acceptor variant C/A;T snv 4.0E-06; 1.2E-05 0.700 1.000 2 2006 2016
dbSNP: rs774047625
rs774047625
ERCC8 ; ERCC8-AS1
1 1.000 0.160 5 60918264 splice donor variant C/G;T snv 4.0E-06 0.700 1.000 2 2006 2015
dbSNP: rs1128503
rs1128503
ABCB1
64 0.564 0.760 7 87550285 synonymous variant A/G snv 0.54 0.63 0.010 1.000 1 2011 2011
dbSNP: rs143367518
rs143367518
ERCC8 ; ERCC8-AS1
1 1.000 0.160 5 60918364 stop gained G/C snv 1.6E-05 3.5E-05 0.700 1.000 1 2010 2010
dbSNP: rs1554073316
rs1554073316
ERCC8
1 1.000 0.160 5 60902509 splice acceptor variant C/T snv 0.700 1.000 1 2010 2010
dbSNP: rs1799983
rs1799983
NOS3
246 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1.000 1 2005 2005
dbSNP: rs2032582
rs2032582
ABCB1
97 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 0.010 1.000 1 2011 2011
dbSNP: rs2266788
rs2266788
ZPR1 ; APOA5
19 0.763 0.440 11 116789970 3 prime UTR variant G/A snv 0.93 0.010 1.000 1 2018 2018
dbSNP: rs4680
rs4680
COMT ; MIR4761
249 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 0.010 1.000 1 2020 2020
dbSNP: rs536368448
rs536368448
NTF3
2 0.925 0.200 12 5494689 missense variant G/A snv 4.0E-06 0.010 1.000 1 2020 2020
dbSNP: rs6265
rs6265
BDNF ; BDNF-AS
272 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 0.010 1.000 1 2020 2020
dbSNP: rs759834365
rs759834365
BDNF ; BDNF-AS
237 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 0.010 1.000 1 2020 2020
dbSNP: rs770804393
rs770804393
DLK1
3 0.882 0.240 14 100734514 missense variant G/A snv 4.0E-06 7.0E-06 0.010 1.000 1 2002 2002
dbSNP: rs893924483
rs893924483
BDNF ; BDNF-AS
23 0.716 0.280 11 27658285 missense variant C/A;T snv 4.0E-06 1.4E-05 0.010 1.000 1 2020 2020
dbSNP: rs1043679457
rs1043679457
ERCC8
33 0.752 0.400 5 60927745 intron variant C/A;G;T snv 0.700 0
dbSNP: rs121434323
rs121434323
ERCC8
2 0.925 0.160 5 60890964 stop gained G/C;T snv 4.0E-06 0.700 0
dbSNP: rs1305258765
rs1305258765
ERCC8
1 1.000 0.160 5 60898275 splice donor variant C/A snv 7.0E-06 0.700 0
dbSNP: rs1476095782
rs1476095782
ERCC8
1 1.000 0.160 5 60928863 splice donor variant C/T snv 8.0E-06 0.700 0