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: rs3129055
rs3129055 		2 1.000 0.120 6 29702484 regulatory region variant A/G snv 0.24 0.700 1.000 1 2009 2009
dbSNP: rs3731239
rs3731239
CDKN2A
10 0.763 0.240 9 21974219 intron variant A/G snv 0.26 0.700 1.000 1 2016 2016
dbSNP: rs1412829
rs1412829
CDKN2B-AS1
14 0.742 0.400 9 22043927 intron variant A/G snv 0.28 0.700 1.000 2 2010 2016
dbSNP: rs1572072
rs1572072 		2 1.000 0.120 13 23553071 intergenic variant G/T snv 0.36 0.700 1.000 1 2010 2010
dbSNP: rs29232
rs29232 		4 0.925 0.240 6 29643654 intergenic variant C/T snv 0.39 0.700 1.000 1 2009 2009
dbSNP: rs31489
rs31489
CLPTM1L
10 0.763 0.320 5 1342599 intron variant C/A snv 0.41 0.700 1.000 1 2016 2016
dbSNP: rs6774494
rs6774494
MECOM
4 0.882 0.160 3 169364845 intron variant G/A snv 0.42 0.700 1.000 2 2010 2016
dbSNP: rs401681
rs401681
CLPTM1L
42 0.620 0.640 5 1321972 intron variant C/T snv 0.48 0.700 1.000 1 2016 2016
dbSNP: rs162171
rs162171
CEP128
1 14 80794033 intron variant A/C snv 0.64 0.700 1.000 1 2019 2019
dbSNP: rs4977756
rs4977756
CDKN2B-AS1
24 0.683 0.440 9 22068653 intron variant G/A snv 0.64 0.700 1.000 1 2016 2016
dbSNP: rs6498114
rs6498114
CIITA ; LOC105371080
2 1.000 0.080 16 10870261 intron variant G/T snv 0.78 0.700 1.000 1 2016 2016