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: rs10057590
rs10057590
LINC02240
1 5 124999554 intron variant A/C snv 0.62 0.700 1.000 1 2018 2018
dbSNP: rs10061387
rs10061387 		1 5 124524355 intron variant A/G snv 0.47 0.700 1.000 1 2018 2018
dbSNP: rs10065159
rs10065159
NEURL1B
1 5 172668864 intron variant T/C snv 0.77 0.700 1.000 1 2018 2018
dbSNP: rs10066711
rs10066711
MEF2C ; MEF2C-AS1
1 5 88894787 intron variant A/T snv 0.52 0.700 1.000 1 2018 2018
dbSNP: rs10073038
rs10073038
CAMK4
1 5 111230823 intron variant A/T snv 0.38 0.700 1.000 1 2018 2018
dbSNP: rs10088255
rs10088255
UBR5
1 8 102355371 intron variant A/T snv 0.55 0.700 1.000 1 2018 2018
dbSNP: rs10098073
rs10098073
TSNARE1
2 1.000 0.040 8 142228143 intron variant C/A snv 0.35 0.700 1.000 1 2018 2018
dbSNP: rs10106406
rs10106406
PTK2
1 8 140996099 intron variant C/A;G snv 0.45 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: rs1011392
rs1011392
TCF4
1 18 55374672 intron variant A/G snv 0.39 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: rs10132779
rs10132779
LOC102724934
1 14 29249690 intron variant A/G snv 0.19 0.700 1.000 1 2018 2018
dbSNP: rs10137343
rs10137343
RBM23
1 14 22913431 intron variant A/T snv 0.56 0.700 1.000 1 2018 2018
dbSNP: rs1015438
rs1015438
SALL1
1 16 51143606 intron variant G/A snv 0.19 0.700 1.000 1 2018 2018
dbSNP: rs10177638
rs10177638 		1 2 62659875 intron variant C/T snv 0.69 0.700 1.000 1 2018 2018
dbSNP: rs10189857
rs10189857
BCL11A
6 1.000 0.080 2 60486100 intron variant A/G snv 0.42 0.700 1.000 1 2018 2018
dbSNP: rs10193498
rs10193498
MAP3K20 ; MAP3K20-AS1
1 2 173229617 intron variant A/C;T snv 0.32 0.700 1.000 1 2018 2018
dbSNP: rs10197780
rs10197780 		1 2 62646060 intron variant T/C snv 0.78 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: rs10202535
rs10202535
TMEM182
1 2 102957679 intron variant T/C snv 0.61 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: rs10206657
rs10206657
LOC105373929
1 2 232597385 intron variant G/A snv 0.19 0.700 1.000 1 2018 2018
dbSNP: rs10208720
rs10208720
PKP4
1 2 158609502 intron variant T/G snv 0.83 0.700 1.000 1 2018 2018