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: rs116621133
rs116621133
KANK4
1 1 62296579 intron variant T/A snv 4.5E-03 0.700 1.000 1 2017 2017
dbSNP: rs12452028
rs12452028
SLC26A11
1 17 80238432 intron variant G/C snv 0.31 0.700 1.000 1 2012 2012
dbSNP: rs146151667
rs146151667
SPAG16
1 2 214319145 intron variant A/G snv 8.0E-03 0.700 1.000 1 2017 2017
dbSNP: rs1545747
rs1545747
MEGF11
3 15 66164979 intron variant G/T snv 0.97 0.700 1.000 1 2017 2017
dbSNP: rs17369571
rs17369571 		1 13 21913486 intergenic variant G/A snv 0.20 0.700 1.000 1 2008 2008
dbSNP: rs1917805
rs1917805 		1 10 49597937 intergenic variant A/G snv 0.41 0.700 1.000 1 2012 2012
dbSNP: rs2019023
rs2019023 		1 19 54547968 upstream gene variant A/C;G;T snv 0.700 1.000 1 2017 2017
dbSNP: rs35019477
rs35019477 		1 9 116409871 intergenic variant AC/-;ACAC;ACACAC;ACACACAC delins 0.700 1.000 1 2017 2017
dbSNP: rs35803309
rs35803309
DNAH11
1 7 21683510 intron variant -/T delins 0.13 0.700 1.000 1 2017 2017
dbSNP: rs6734238
rs6734238 		8 1.000 0.080 2 113083453 upstream gene variant A/G snv 0.39 0.700 1.000 1 2012 2012
dbSNP: rs6743376
rs6743376
IL1F10
2 2 113074756 missense variant C/A snv 0.69 0.69 0.700 1.000 1 2014 2014