Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12726299
SLC22A15
1.000 0.040 1 115983051 intron variant G/A snv 0.46 1
rs13166776 1.000 0.040 5 25971247 intron variant T/C snv 0.28 1
rs1344706
ZNF804A
0.701 0.160 2 184913701 intron variant A/C;T snv 1
rs1409313
CUEDC2
1.000 0.040 10 102431844 intron variant T/C snv 0.85 1
rs1429793
NELL1 ; LOC105376585
1.000 0.040 11 20904710 intron variant G/C;T snv 1
rs1475531
MACROD2 ; MACROD2-AS1
1.000 0.040 20 14886776 intron variant G/T snv 0.62 1
rs155806
PCDHA5 ; PCDHA7 ; PCDHA1 ; PCDHAC1 ; PCDHA10 ; PCDHA6 ; PCDHA11 ; PCDHAC2 ; PCDHA12 ; PCDHA13 ; PCDHA4 ; PCDHA9 ; PCDHA3 ; PCDHA2 ; PCDHA8
1.000 0.040 5 140970255 intron variant A/G snv 8.9E-02 1
rs16919315
TMEM132B
1.000 0.040 12 125599817 intron variant C/A;G;T snv 1
rs16976358
LINC00907
0.827 0.080 18 42611606 intron variant T/C snv 1.0E-02 1
rs17007739 1.000 0.040 4 83920097 intron variant T/G snv 0.38 1
rs17134117
SDK1
1.000 0.040 7 3991432 intron variant C/T snv 9.1E-02 1
rs1718101
CNTNAP2
1.000 0.040 7 146425696 intron variant T/C;G snv 1
rs1879532
ERBB4
1.000 0.040 2 211574587 intron variant T/A;C;G snv 1
rs1930165
LOC105378311 ; PCDH15
1.000 0.040 10 54542170 intron variant G/A;C snv 1
rs2056412
FAM135B
1.000 0.040 8 138401090 intron variant T/C snv 0.14 1
rs2150291
SYNE2
1.000 0.040 14 63864705 intron variant T/C snv 0.81 1
rs263025
YEATS2-AS1 ; YEATS2
1.000 0.040 3 183809830 intron variant T/C snv 0.45 1
rs263035
YEATS2
1.000 0.040 3 183805869 intron variant A/G snv 0.44 1
rs2710102
CNTNAP2
0.790 0.120 7 147877298 intron variant A/G;T snv 1
rs2836439
ERG
1.000 0.040 21 38493226 intron variant C/T snv 0.16 1
rs289932 1.000 0.040 2 151149511 intron variant C/T snv 0.39 1
rs3782000
ZBTB16
1.000 0.040 11 114202153 intron variant C/T snv 0.18 1
rs3797817
FER
1.000 0.040 5 108948641 intron variant A/C;G snv 1
rs3827735
TRIM33
1.000 0.040 1 114510087 intron variant C/A;T snv 1
rs4141463
MACROD2
0.925 0.040 20 14766825 intron variant T/C snv 0.50 1