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: rs10510452
rs10510452 		2 1.000 0.120 3 16583541 downstream gene variant A/G snv 0.22 0.800 1.000 4 2013 2017
dbSNP: rs2072499
rs2072499
SLC25A44
3 1.000 0.120 1 156199819 non coding transcript exon variant A/G snv 0.34 0.43 0.800 1.000 4 2013 2017
dbSNP: rs2720460
rs2720460
CENPE
2 1.000 0.120 4 103133529 intron variant A/G snv 0.35 0.800 1.000 4 2013 2017
dbSNP: rs3790672
rs3790672
UCK2
2 1.000 0.120 1 165904155 non coding transcript exon variant T/C snv 0.24 0.800 1.000 4 2013 2017
dbSNP: rs9905704
rs9905704
SEPTIN4-AS1
2 1.000 0.120 17 58555182 intron variant G/T snv 0.77 0.810 1.000 4 2013 2017
dbSNP: rs12699477
rs12699477
MAD1L1
2 1.000 0.120 7 1929317 intron variant T/C snv 0.28 0.800 1.000 3 2013 2017
dbSNP: rs137853078
rs137853078
STK11
3 0.925 0.120 19 1220396 missense variant G/A snv 0.700 1.000 3 1998 2008
dbSNP: rs17021463
rs17021463
HPGDS
2 1.000 0.120 4 94303661 intron variant T/G snv 0.57 0.800 1.000 3 2013 2017
dbSNP: rs2195987
rs2195987 		1 1.000 0.120 19 23966743 intergenic variant C/G;T snv 0.700 1.000 3 2015 2017
dbSNP: rs4561483
rs4561483
BCAR4
1 1.000 0.120 16 11826180 intron variant A/G;T snv 0.710 1.000 3 2015 2017
dbSNP: rs4888262
rs4888262
RFWD3
2 1.000 0.120 16 74636560 synonymous variant C/T snv 0.54 0.59 0.800 1.000 3 2013 2017
dbSNP: rs55637647
rs55637647
ZFPM1
1 1.000 0.120 16 88482856 intron variant C/G snv 0.47 0.710 1.000 3 2015 2017
dbSNP: rs7010162
rs7010162
PRDM14
2 1.000 0.120 8 70064270 intron variant C/T snv 0.52 0.800 1.000 3 2013 2017
dbSNP: rs755383
rs755383
DMRT1
7 0.807 0.120 9 863635 intron variant C/T snv 0.54 0.800 1.000 3 2013 2017
dbSNP: rs8046148
rs8046148 		2 1.000 0.120 16 50109033 intron variant A/G;T snv 0.800 1.000 3 2013 2017
dbSNP: rs11705932
rs11705932
TFDP2
1 1.000 0.120 3 142100008 intron variant C/T snv 0.20 0.710 1.000 2 2015 2017
dbSNP: rs1510272
rs1510272 		1 1.000 0.120 3 156582935 regulatory region variant C/T snv 0.25 0.700 1.000 2 2017 2017
dbSNP: rs2839186
rs2839186
MCM3AP
2 1.000 0.120 21 46270154 intron variant C/T snv 0.42 0.800 1.000 2 2013 2017
dbSNP: rs3782181
rs3782181
KITLG
4 0.882 0.120 12 88559784 intron variant C/A snv 0.65 0.700 1.000 2 2017 2017
dbSNP: rs7040024
rs7040024
DMRT1
4 0.925 0.120 9 845516 intron variant A/C;G snv 0.700 1.000 2 2017 2017
dbSNP: rs1009647
rs1009647
ATG14
2 1.000 0.120 14 55413329 upstream gene variant G/A snv 0.24 0.700 1.000 1 2017 2017
dbSNP: rs10146204
rs10146204 		2 1.000 0.120 14 64352051 non coding transcript exon variant G/A snv 0.45 0.010 1.000 1 2012 2012
dbSNP: rs11071896
rs11071896
ZWILCH
2 1.000 0.120 15 66528912 missense variant A/G snv 0.23 0.20 0.700 1.000 1 2017 2017
dbSNP: rs11155671
rs11155671
KATNA1
1 1.000 0.120 6 149650996 upstream gene variant G/A snv 0.46 0.700 1.000 1 2017 2017
dbSNP: rs11202586
rs11202586 		1 1.000 0.120 10 87852267 intergenic variant T/C snv 0.18 0.010 1.000 1 2013 2013