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: rs13129697
rs13129697
SLC2A9
5 0.925 0.120 4 9925343 intron variant T/G snv 0.39 0.800 1.000 6 2009 2018
dbSNP: rs1471633
rs1471633 		3 0.925 0.120 1 145711327 upstream gene variant T/G snv 0.43 0.800 1.000 3 2009 2019
dbSNP: rs10910845
rs10910845 		3 0.925 0.120 1 145711946 upstream gene variant T/G snv 0.44 0.800 1.000 2 2009 2019
dbSNP: rs4698036
rs4698036 		4 0.925 0.120 4 10329670 intergenic variant T/G snv 0.21 0.800 1.000 2 2009 2011
dbSNP: rs10418164
rs10418164
CEP89
1 19 32920233 intron variant T/G snv 0.64 0.700 1.000 1 2019 2019
dbSNP: rs10438961
rs10438961 		1 18 45199142 intergenic variant T/G snv 0.25 0.700 1.000 1 2019 2019
dbSNP: rs10805356
rs10805356 		3 0.925 0.120 4 10139978 downstream gene variant T/G snv 0.42 0.700 1.000 1 2009 2009
dbSNP: rs10939663
rs10939663
SLC2A9
3 0.925 0.120 4 10030892 intron variant T/G snv 0.20 0.700 1.000 1 2009 2009
dbSNP: rs13103690
rs13103690
SLC2A9
3 0.925 0.120 4 9971154 intron variant T/G snv 0.57 0.700 1.000 1 2009 2009
dbSNP: rs13115121
rs13115121
SLC2A9
3 0.925 0.120 4 9895718 intron variant T/G snv 0.39 0.700 1.000 1 2009 2009
dbSNP: rs148015593
rs148015593
MLXIP
1 12 122085762 intron variant T/G snv 0.52 0.700 1.000 1 2019 2019
dbSNP: rs16886173
rs16886173 		2 8 114608231 intergenic variant T/G snv 7.5E-02 0.700 1.000 1 2015 2015
dbSNP: rs17406107
rs17406107 		3 0.925 0.120 4 10261756 upstream gene variant T/G snv 0.18 0.700 1.000 1 2009 2009
dbSNP: rs17419612
rs17419612 		3 0.925 0.120 4 10335639 intergenic variant T/G snv 0.20 0.700 1.000 1 2009 2009
dbSNP: rs1997672
rs1997672
CARMIL1
4 0.925 0.120 6 25617316 intron variant T/G snv 0.28 0.700 1.000 1 2009 2009
dbSNP: rs2192084
rs2192084 		3 0.925 0.120 4 10345427 intergenic variant T/G snv 0.62 0.700 1.000 1 2009 2009
dbSNP: rs2241470
rs2241470
WDR1
3 0.925 0.120 4 10082946 intron variant T/G snv 0.31 0.700 1.000 1 2009 2009
dbSNP: rs2241475
rs2241475
WDR1
1 4 10084564 intron variant T/G snv 0.35 0.33 0.700 1.000 1 2009 2009
dbSNP: rs2867112
rs2867112 		3 2 651349 intergenic variant T/G snv 0.18 0.700 1.000 1 2019 2019
dbSNP: rs35258188
rs35258188
WDR72
4 1.000 0.040 15 53705141 missense variant T/G snv 3.5E-03 1.5E-02 0.700 1.000 1 2018 2018
dbSNP: rs4422413
rs4422413
ZNF518B
3 0.925 0.120 4 10441760 3 prime UTR variant T/G snv 0.28 0.700 1.000 1 2009 2009
dbSNP: rs4697936
rs4697936
LOC105374478
3 0.925 0.120 4 10147971 upstream gene variant T/G snv 0.42 0.700 1.000 1 2009 2009
dbSNP: rs6119510
rs6119510
NCOA6
1 20 34699978 intron variant T/G snv 0.36 0.700 1.000 1 2019 2019
dbSNP: rs6449144
rs6449144
SLC2A9
3 0.925 0.120 4 9943026 intron variant T/G snv 0.75 0.700 1.000 1 2009 2009
dbSNP: rs6449155
rs6449155
SLC2A9
3 0.925 0.120 4 9954923 intron variant T/G snv 0.49 0.700 1.000 1 2009 2009