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: rs1394371
rs1394371 		4 0.925 0.080 15 78432127 intergenic variant C/T snv 0.22 0.700 1.000 4 2008 2012
dbSNP: rs1800734
rs1800734
MLH1 ; EPM2AIP1
30 0.653 0.400 3 36993455 5 prime UTR variant G/A snv 0.22 0.040 1.000 4 2011 2017
dbSNP: rs1996371
rs1996371
CHRNB4 ; LOC112268142
4 1.000 0.080 15 78664464 intron variant T/C snv 0.28 0.700 1.000 4 2008 2012
dbSNP: rs2036534
rs2036534
HYKK
8 0.827 0.080 15 78534606 3 prime UTR variant T/C snv 0.26 0.710 1.000 4 2008 2012
dbSNP: rs2853677
rs2853677
TERT
19 0.724 0.240 5 1287079 3 prime UTR variant G/A snv 0.63 0.040 1.000 4 2016 2019
dbSNP: rs4646903
rs4646903
CYP1A1
36 0.630 0.640 15 74719300 downstream gene variant A/G;T snv 0.18 0.040 0.750 4 2010 2016
dbSNP: rs4887077
rs4887077
CHRNB4 ; LOC112268142
4 1.000 0.080 15 78686022 intron variant C/T snv 0.28 0.700 1.000 4 2008 2012
dbSNP: rs6495314
rs6495314
CHRNB4 ; LOC112268142
4 0.925 0.080 15 78668187 intron variant A/C snv 0.35 0.700 1.000 4 2008 2012
dbSNP: rs6983267
rs6983267
POU5F1B ; CASC8 ; PCAT1 ; CCAT2
62 0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 0.040 1.000 4 2008 2017
dbSNP: rs762551
rs762551
CYP1A2
23 0.701 0.400 15 74749576 intron variant C/A snv 0.67 0.040 1.000 4 2012 2014
dbSNP: rs8042374
rs8042374
CHRNA3
10 0.807 0.200 15 78615690 intron variant A/G snv 0.29 0.710 1.000 4 2008 2012
dbSNP: rs12910984
rs12910984
CHRNA3
8 0.827 0.080 15 78599285 intron variant G/A;C;T snv 0.710 1.000 3 2009 2012
dbSNP: rs1760944
rs1760944
APEX1 ; OSGEP
26 0.672 0.480 14 20454990 non coding transcript exon variant T/C;G snv 0.030 1.000 3 2009 2014
dbSNP: rs1800624
rs1800624
AGER ; PBX2
33 0.658 0.480 6 32184610 upstream gene variant A/G;T snv 0.030 1.000 3 2013 2017
dbSNP: rs1800796
rs1800796
IL6 ; STEAP1B ; IL6-AS1
74 0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 0.030 0.667 3 2014 2018
dbSNP: rs2031920
rs2031920
CYP2E1 ; LOC107984284
20 0.695 0.240 10 133526341 non coding transcript exon variant C/T snv 3.1E-02 0.030 1.000 3 2012 2016
dbSNP: rs2298881
rs2298881
ERCC1
25 0.653 0.400 19 45423658 intron variant C/A;T snv 0.030 1.000 3 2011 2014
dbSNP: rs2352028
rs2352028
GPC5
6 0.851 0.080 13 91792975 intron variant C/G;T snv 0.030 1.000 3 2010 2015
dbSNP: rs2853669
rs2853669
TERT
35 0.649 0.320 5 1295234 upstream gene variant A/G snv 0.25 0.030 1.000 3 2013 2018
dbSNP: rs2868371
rs2868371
HSPB1
6 0.827 0.120 7 76301442 upstream gene variant C/G snv 0.22 0.030 0.667 3 2015 2019
dbSNP: rs3743073
rs3743073
CHRNA3
11 0.807 0.120 15 78617197 intron variant G/T snv 0.61 0.030 0.667 3 2010 2013
dbSNP: rs4645981
rs4645981
CASP9 ; DNAJC16
11 0.790 0.160 1 15524988 intron variant G/A;C snv 0.030 1.000 3 2010 2013
dbSNP: rs4887053
rs4887053 		4 0.925 0.080 15 78420357 regulatory region variant A/C;T snv 0.700 1.000 3 2008 2012
dbSNP: rs664143
rs664143
ATM ; C11orf65
8 0.807 0.160 11 108354934 3 prime UTR variant A/G;T snv 0.030 1.000 3 2012 2017
dbSNP: rs664677
rs664677
ATM
8 0.807 0.160 11 108272455 intron variant C/A;T snv 0.65 0.030 1.000 3 2012 2017