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: rs112599895
rs112599895 		1 1.000 0.080 4 110735436 intergenic variant A/G snv 1.2E-02 0.700 1.000 1 2018 2018
dbSNP: rs113819537
rs113819537
SSPN
1 1.000 0.080 12 26195496 5 prime UTR variant C/G snv 0.21 0.700 1.000 1 2018 2018
dbSNP: rs114904067
rs114904067 		1 1.000 0.080 4 111683665 intergenic variant G/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs11590635
rs11590635
AGBL4
1 1.000 0.080 1 48844092 intron variant G/A snv 1.6E-02 0.700 1.000 1 2018 2018
dbSNP: rs11614818
rs11614818 		1 1.000 0.080 12 55662031 upstream gene variant C/T snv 0.49 0.700 1.000 1 2018 2018
dbSNP: rs11658278
rs11658278
ZPBP2
1 1.000 0.080 17 39874911 intron variant T/C snv 0.46 0.700 1.000 1 2018 2018
dbSNP: rs117640426
rs117640426 		1 1.000 0.080 12 25905670 intergenic variant T/C snv 1.1E-02 0.700 1.000 1 2017 2017
dbSNP: rs11768850
rs11768850
SUN1
1 1.000 0.080 7 836590 intron variant C/T snv 0.40 0.700 1.000 1 2018 2018
dbSNP: rs11773884
rs11773884
CDK6
1 1.000 0.080 7 92655809 intron variant A/G snv 0.36 0.700 1.000 1 2018 2018
dbSNP: rs118159104
rs118159104
CRAMP1
1 1.000 0.080 16 1626803 intron variant T/A;G snv 0.700 1.000 1 2018 2018
dbSNP: rs11846704
rs11846704 		1 1.000 0.080 14 34717488 upstream gene variant C/T snv 0.35 0.700 1.000 1 2018 2018
dbSNP: rs12122060
rs12122060
LINC01681
1 1.000 0.080 1 170224718 intron variant T/A snv 7.9E-02 0.700 1.000 1 2018 2018
dbSNP: rs12129500
rs12129500
IL6R
1 1.000 0.080 1 154451288 intron variant T/C snv 0.60 0.700 1.000 1 2018 2018
dbSNP: rs12142379
rs12142379
PRRX1
1 1.000 0.080 1 170724397 intron variant T/C snv 4.7E-02 0.700 1.000 1 2018 2018
dbSNP: rs12188351
rs12188351
SLIT3
2 0.925 0.120 5 168959084 intron variant G/A snv 3.8E-02 0.700 1.000 1 2018 2018
dbSNP: rs12208899
rs12208899 		1 1.000 0.080 6 133153164 downstream gene variant G/A snv 0.15 0.700 1.000 1 2018 2018
dbSNP: rs12245149
rs12245149
REEP3
1 1.000 0.080 10 63561387 intron variant C/A snv 0.48 0.700 1.000 1 2018 2018
dbSNP: rs12298484
rs12298484
CCDC92 ; DNAH10 ; DNAH10OS
1 1.000 0.080 12 123934127 non coding transcript exon variant C/T snv 0.28 0.32 0.700 1.000 1 2018 2018
dbSNP: rs12310617
rs12310617 		16 0.851 0.120 12 3060327 intergenic variant C/T snv 0.11 0.700 1.000 1 2016 2016
dbSNP: rs12369179
rs12369179
ZCCHC8
16 0.851 0.120 12 122479003 intron variant C/T snv 5.9E-02 0.700 1.000 1 2016 2016
dbSNP: rs12420422
rs12420422 		16 0.851 0.120 11 123009573 intergenic variant G/A snv 3.4E-02 0.700 1.000 1 2016 2016
dbSNP: rs12426679
rs12426679
LOC105369844
1 1.000 0.080 12 75844207 intron variant C/T snv 0.40 0.700 1.000 1 2018 2018
dbSNP: rs12579302
rs12579302
ATP2B1
19 0.851 0.120 12 89656726 intron variant A/G snv 0.15 0.700 1.000 1 2016 2016
dbSNP: rs12591736
rs12591736 		1 1.000 0.080 15 70161800 intergenic variant G/A;C;T snv 0.700 1.000 1 2018 2018
dbSNP: rs12604076
rs12604076
CYTH1
1 1.000 0.080 17 78777556 intron variant T/C snv 0.46 0.700 1.000 1 2018 2018