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: rs10009715
rs10009715
LOC105377535
1 4 171510209 intron variant T/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs10055216
rs10055216
RANBP17
1 5 170981562 intron variant A/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs10107533
rs10107533
CSGALNACT1
1 8 19521910 intron variant C/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs10122976
rs10122976
KCNT1
1 9 135751066 intron variant C/A;T snv 0.47; 1.2E-05 0.700 1.000 1 2018 2018
dbSNP: rs10161821
rs10161821
LINC00375 ; LOC105370291
1 13 85129514 intergenic variant G/A;C;T snv 0.700 1.000 1 2018 2018
dbSNP: rs10183150
rs10183150
LONRF2
1 2 100322655 upstream gene variant A/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs1019914
rs1019914
SDK1
1 7 3672560 intron variant G/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs10205421
rs10205421
VRK2
1 2 58070529 intron variant G/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs10211312
rs10211312
TMEM17 ; LOC105374764
1 2 62466982 downstream gene variant A/C;T snv 0.700 1.000 1 2018 2018
dbSNP: rs10223255
rs10223255 		1 5 92705821 intergenic variant A/C;G snv 0.700 1.000 1 2018 2018
dbSNP: rs10268735
rs10268735
POU6F2 ; LOC105375239
1 7 39336423 intron variant A/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs10459501
rs10459501
MDGA2
1 14 47368546 intron variant C/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs10462889
rs10462889
TENM2
1 5 167239713 intergenic variant G/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs10497239
rs10497239
FIGN
1 2 163674795 intron variant T/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs1060709
rs1060709
B3GLCT
1 13 31329697 3 prime UTR variant G/A;T snv 1.2E-05; 0.64 0.700 1.000 1 2018 2018
dbSNP: rs10734924
rs10734924
KNTC1
1 12 122534347 intron variant T/A;G snv 0.700 1.000 1 2018 2018
dbSNP: rs10740128
rs10740128
JMJD1C
1 10 63490783 intron variant A/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs10740140
rs10740140 		1 10 63759994 intron variant A/C;G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs10757463
rs10757463 		1 9 23967942 intergenic variant A/C;G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs10786832
rs10786832
SORCS3
1 10 104858690 intron variant C/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs10789442
rs10789442
KDM4A
1 1 43674404 intron variant A/C;G snv 0.700 1.000 1 2018 2018
dbSNP: rs10792472
rs10792472 		1 11 80194928 intergenic variant G/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs10810107
rs10810107
NFIB
1 9 14195828 intron variant C/A;G snv 0.700 1.000 1 2018 2018
dbSNP: rs10820741
rs10820741
CDC14B
1 9 96505271 intron variant T/C;G snv 0.700 1.000 1 2018 2018
dbSNP: rs1083845
rs1083845
LINC01170
1 5 124257166 intron variant A/G;T snv 0.700 1.000 1 2018 2018