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: rs10157710
rs10157710 		1 1 47496019 downstream gene variant C/T snv 0.78 0.700 1.000 1 2018 2018
dbSNP: rs10207567
rs10207567
ICA1L
1 2 202850250 intron variant G/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs11162351
rs11162351
AK5
1 1 77479047 intron variant C/G snv 0.31 0.700 1.000 1 2018 2018
dbSNP: rs1124694
rs1124694
LINC02752
1 11 11077129 intron variant A/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs112607182
rs112607182 		2 3 170309619 downstream gene variant C/T snv 5.3E-02 0.700 1.000 1 2018 2018
dbSNP: rs11264327
rs11264327 		1 1 155122631 downstream gene variant G/A;C;T snv 0.700 1.000 1 2018 2018
dbSNP: rs1145074
rs1145074
SPATA5L1
1 15 45411626 intron variant T/A;G snv 0.45 0.700 1.000 1 2018 2018
dbSNP: rs12032996
rs12032996 		1 1 33454985 intergenic variant G/A snv 0.12 0.700 1.000 1 2018 2018
dbSNP: rs12727104
rs12727104 		1 1 171454028 intergenic variant G/A snv 8.3E-02 0.700 1.000 1 2018 2018
dbSNP: rs12727980
rs12727980
LINC00862
1 1 200289967 intron variant C/T snv 0.54 0.700 1.000 1 2018 2018
dbSNP: rs1276720
rs1276720
CUBN
1 10 16929427 intron variant C/T snv 0.65 0.700 1.000 1 2018 2018
dbSNP: rs13394343
rs13394343 		1 2 85527219 intergenic variant C/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs146311723
rs146311723
USP3
2 1.000 0.080 15 63512308 intron variant T/C snv 0.14 0.700 1.000 1 2018 2018
dbSNP: rs16943246
rs16943246 		1 15 45428399 upstream gene variant G/A snv 0.29 0.700 1.000 1 2018 2018
dbSNP: rs17158386
rs17158386 		2 7 29765745 regulatory region variant G/A snv 0.19 0.700 1.000 1 2018 2018
dbSNP: rs17368443
rs17368443
SBF2
1 11 10275289 intron variant G/C snv 5.3E-02 0.700 1.000 1 2018 2018
dbSNP: rs183131780
rs183131780
LOC105373914 ; LOC107985992
1 2 225820170 intergenic variant C/T snv 1.0E-03 0.700 1.000 1 2018 2018
dbSNP: rs185291443
rs185291443 		1 2 226120788 intergenic variant C/A;G snv 0.700 1.000 1 2019 2019
dbSNP: rs189107782
rs189107782
FRG1-DT
1 4 189807855 intron variant C/T snv 1.5E-03 0.700 1.000 1 2018 2018
dbSNP: rs2023844
rs2023844
HOTTIP
1 7 27203619 intron variant G/A snv 0.93 0.700 1.000 1 2018 2018
dbSNP: rs2338796
rs2338796
FBXL20
1 17 39399374 intron variant A/G snv 0.27 0.700 1.000 1 2018 2018
dbSNP: rs2470893
rs2470893
CYP1A1
8 0.882 0.160 15 74727108 upstream gene variant C/T snv 0.20 0.700 1.000 1 2018 2018
dbSNP: rs2472297
rs2472297 		9 0.882 0.160 15 74735539 intergenic variant C/T snv 0.16 0.700 1.000 1 2018 2018
dbSNP: rs2601006
rs2601006
CCT2 ; MIR3913-1
1 12 69585737 5 prime UTR variant C/T snv 0.39 0.700 1.000 1 2018 2018
dbSNP: rs28601761
rs28601761 		13 1.000 0.040 8 125487789 intron variant C/G snv 0.37 0.700 1.000 1 2018 2018