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: rs10993994
rs10993994
MSMB
15 0.763 0.280 10 46046326 5 prime UTR variant A/G snv 0.54 0.800 1.000 3 2010 2017
dbSNP: rs2735839
rs2735839 		7 0.827 0.160 19 50861367 upstream gene variant A/C;G snv 0.800 1.000 3 2010 2018
dbSNP: rs1058205
rs1058205
KLK3
3 0.925 0.080 19 50860142 3 prime UTR variant C/T snv 0.75 0.74 0.800 1.000 2 2010 2014
dbSNP: rs11067228
rs11067228 		3 0.925 0.080 12 114656455 downstream gene variant A/G snv 0.37 0.800 1.000 2 2010 2017
dbSNP: rs11084596
rs11084596 		3 1.000 0.040 19 31614073 regulatory region variant T/C snv 0.35 0.700 1.000 2 2017 2018
dbSNP: rs17632542
rs17632542
KLK3
5 0.925 0.080 19 50858501 missense variant T/C snv 5.5E-02 4.9E-02 0.800 1.000 2 2010 2017
dbSNP: rs266849
rs266849
LOC105372441
4 0.925 0.080 19 50845834 intron variant G/A snv 0.82 0.800 1.000 2 2010 2017
dbSNP: rs10023685
rs10023685 		1 4 156613097 intergenic variant C/A;G snv 0.700 1.000 1 2017 2017
dbSNP: rs10486567
rs10486567
JAZF1
9 0.851 0.120 7 27936944 intron variant G/A snv 0.28 0.700 1.000 1 2017 2017
dbSNP: rs10505477
rs10505477
POU5F1B ; CASC8 ; PCAT1
31 0.658 0.400 8 127395198 intron variant A/G snv 0.40 0.700 1.000 1 2017 2017
dbSNP: rs10734875
rs10734875
ATF7IP
1 12 14389607 intron variant A/G;T snv 0.700 1.000 1 2013 2013
dbSNP: rs10749415
rs10749415 		1 10 121425789 intergenic variant G/A;C snv 0.700 1.000 1 2017 2017
dbSNP: rs10772782
rs10772782
ATF7IP
1 12 14439909 intron variant A/G snv 0.29 0.700 1.000 1 2013 2013
dbSNP: rs10788160
rs10788160 		2 10 121274035 intergenic variant G/A snv 0.19 0.800 1.000 1 2010 2010
dbSNP: rs10855058
rs10855058
KLF8
1 X 55910389 intron variant A/G snv 0.700 1.000 1 2017 2017
dbSNP: rs10886902
rs10886902 		1 10 121289750 regulatory region variant T/C snv 0.19 0.700 1.000 1 2017 2017
dbSNP: rs11055956
rs11055956
ATF7IP
1 12 14381492 intron variant G/A;C snv 0.700 1.000 1 2013 2013
dbSNP: rs11055980
rs11055980
ATF7IP
3 1.000 0.040 12 14458588 intron variant C/T snv 0.40 0.700 1.000 1 2013 2013
dbSNP: rs11199879
rs11199879 		3 1.000 0.040 10 121285698 regulatory region variant T/C snv 0.18 0.700 1.000 1 2018 2018
dbSNP: rs11263761
rs11263761
HNF1B
2 1.000 0.080 17 37737784 intron variant A/G snv 0.44 0.700 1.000 1 2017 2017
dbSNP: rs11651052
rs11651052
HNF1B
7 0.851 0.200 17 37742390 intron variant G/A snv 0.50 0.700 1.000 1 2018 2018
dbSNP: rs11665748
rs11665748
LOC105372441
1 19 50851141 upstream gene variant G/A snv 0.63 0.700 1.000 1 2017 2017
dbSNP: rs116940348
rs116940348 		1 10 22292652 intergenic variant G/A;T snv 0.700 1.000 1 2017 2017
dbSNP: rs12285347
rs12285347
MMP7
1 11 102525876 intron variant T/A;C snv 0.700 1.000 1 2017 2017
dbSNP: rs12409639
rs12409639
SLC45A3
1 1 205669094 intron variant G/A snv 8.8E-02 0.800 1.000 1 2013 2013