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: rs10132280
rs10132280 		6 14 25458973 intergenic variant C/A snv 0.37 0.700 1.000 1 2015 2015
dbSNP: rs10200566
rs10200566
ADCY3
1 2 24907593 intron variant T/G snv 0.54 0.700 1.000 1 2019 2019
dbSNP: rs10835188
rs10835188
LIN7C
2 1.000 0.120 11 27501639 intron variant G/T snv 0.68 0.700 1.000 1 2015 2015
dbSNP: rs10846580
rs10846580
CCDC92 ; DNAH10 ; DNAH10OS
1 12 123930906 intron variant T/C snv 0.45 0.700 1.000 1 2019 2019
dbSNP: rs10929925
rs10929925 		3 2 6015425 intergenic variant C/A;T snv 0.700 1.000 1 2015 2015
dbSNP: rs10938397
rs10938397 		19 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 0.700 1.000 1 2015 2015
dbSNP: rs11057405
rs11057405
CLIP1
2 12 122297350 intron variant G/A;C snv 0.700 1.000 1 2015 2015
dbSNP: rs11152213
rs11152213 		4 1.000 0.080 18 60185715 intergenic variant A/C;T snv 0.700 1.000 1 2019 2019
dbSNP: rs11165623
rs11165623 		2 1 96427444 intergenic variant G/A;T snv 0.700 1.000 1 2015 2015
dbSNP: rs113191842
rs113191842
FTO
5 16 53783406 intron variant G/A snv 9.4E-02 0.700 1.000 1 2017 2017
dbSNP: rs11607976
rs11607976 		2 11 69464343 upstream gene variant C/G;T snv 0.700 1.000 1 2015 2015
dbSNP: rs11672660
rs11672660
GIPR ; MIR642B
5 19 45676926 intron variant C/T snv 0.18 0.17 0.700 1.000 1 2015 2015
dbSNP: rs11676272
rs11676272
ADCY3
5 1.000 0.040 2 24918669 missense variant A/G snv 0.47 0.57 0.700 1.000 1 2015 2015
dbSNP: rs117614852
rs117614852
TTC39B
1 9 15279395 intron variant G/T snv 3.6E-03 0.700 1.000 1 2017 2017
dbSNP: rs11863065
rs11863065 		3 16 82293200 intergenic variant G/A snv 7.3E-02 0.700 1.000 1 2012 2012
dbSNP: rs11873305
rs11873305 		2 1.000 0.080 18 60381959 intron variant A/C snv 0.12 0.700 1.000 1 2015 2015
dbSNP: rs12086130
rs12086130
FAF1
1 1 50707931 intron variant C/T snv 0.12 0.700 1.000 1 2015 2015
dbSNP: rs12146733
rs12146733
FAIM2
3 12 49876581 intron variant G/C;T snv 0.700 1.000 1 2017 2017
dbSNP: rs12446632
rs12446632
LOC105371116
7 1.000 0.080 16 19924067 intergenic variant G/A snv 0.11 0.700 1.000 1 2015 2015
dbSNP: rs12936587
rs12936587 		5 0.882 0.080 17 17640408 regulatory region variant G/A snv 0.38 0.700 1.000 1 2015 2015
dbSNP: rs1294409
rs1294409
LOC101928004
2 6 6738122 intron variant C/T snv 0.63 0.700 1.000 1 2015 2015
dbSNP: rs12967135
rs12967135 		8 18 60181790 intergenic variant G/A snv 0.24 0.700 1.000 1 2017 2017
dbSNP: rs13098327
rs13098327
CADM2
2 3 85771031 intron variant G/A snv 0.15 0.700 1.000 1 2015 2015
dbSNP: rs1320330
rs1320330 		2 2 622225 intergenic variant T/A;G snv 0.700 1.000 1 2017 2017
dbSNP: rs1351394
rs1351394
HMGA2
5 12 65958046 3 prime UTR variant T/C;G snv 0.700 1.000 1 2015 2015