Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10013443
PALLD
1.000 0.080 4 168685769 intron variant T/C snv 3.4E-02 1
rs10024442
TMEM131L
1.000 0.080 4 153570903 intron variant T/G snv 0.13 1
rs10032741 1.000 0.080 4 44958427 intergenic variant T/A;C snv 1
rs10035360 1.000 0.080 5 34604531 regulatory region variant C/T snv 0.19 1
rs10045595
TENM2
1.000 0.080 5 167802999 intron variant T/G snv 0.36 1
rs10049436 1.000 0.080 3 165771478 intron variant C/T snv 8.1E-02 2
rs10091183 1.000 0.080 8 33215980 regulatory region variant A/G snv 4.6E-02 1
rs10094069
CSMD3
1.000 0.080 8 113022302 intron variant C/T snv 0.59 1
rs1009449
LOC105376617
1.000 0.080 11 33684620 intron variant A/G snv 4.2E-03 1
rs1011356 1.000 0.080 14 76678871 intron variant C/A;G snv 1
rs10160659
DCHS1
1.000 0.080 11 6644463 intron variant A/C snv 5.5E-02 1
rs10200800
KCNE4
1.000 0.080 2 223088118 intron variant T/C snv 0.75 1
rs10226621
SDK1
1.000 0.080 7 4068008 intron variant A/C;G snv 1
rs10240026
LOC105379749
1.000 0.080 7 142491501 upstream gene variant A/T snv 6.8E-02 1
rs10418441
COLGALT1
1.000 0.080 19 17569292 intron variant C/A;T snv 1
rs10484565
TAP2
0.925 0.200 6 32827255 3 prime UTR variant G/A snv 6.1E-02 2
rs10487465
GRM8
1.000 0.080 7 127056727 intron variant T/C snv 7.9E-02 1
rs10490165
NRXN1
1.000 0.080 2 50961428 intron variant T/A;C snv 1
rs10775354
RBFOX1
1.000 0.080 16 6757689 intron variant A/C;T snv 1
rs10780661
SLC28A3
1.000 0.080 9 84311392 intron variant A/G;T snv 1
rs1086603 0.882 0.120 1 147816164 intergenic variant G/A snv 3.4E-02 3
rs10894993 0.925 0.080 11 100627998 intergenic variant T/G snv 4.7E-02 2
rs10915020 1.000 0.080 1 34692115 intergenic variant T/A snv 0.10 1
rs10918931 1.000 0.080 1 168592853 intergenic variant T/C snv 0.61 1
rs10944489
MAP3K7
1.000 0.080 6 90554374 intron variant G/A snv 3.6E-02 1