Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1007837
GAB2
1.000 0.080 11 78230030 intron variant T/C snv 0.30 1
rs10078434 1.000 0.080 5 138496342 intergenic variant A/T snv 0.13 1
rs10098778
NDUFAF6
1.000 0.080 8 94979792 intron variant C/A;T snv 1
rs10109834
PTK2B
1.000 0.080 8 27354759 intron variant A/C snv 0.44 1
rs10119
TOMM40
0.925 0.080 19 44903416 3 prime UTR variant G/A snv 0.28 4
rs10139154
SCFD1
0.925 0.120 14 30678292 intron variant C/T snv 0.46 1
rs10194375
BIN1
1.000 0.080 2 127082205 intron variant C/A;T snv 1
rs10207628
BIN1
0.925 0.120 2 127094445 intron variant G/A;C snv 2
rs10222981 0.925 0.080 4 6759326 upstream gene variant G/T snv 0.14 2
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 4
rs1026254
MS4A4A
1.000 0.080 11 60262984 intron variant T/A;C snv 1
rs1026255
MS4A4A
1.000 0.080 11 60262476 intron variant G/A snv 0.67 1
rs1033301
VSNL1
1.000 0.080 2 17592731 intron variant A/C snv 0.11 1
rs1036819
ZFAT-AS1 ; ZFAT
0.925 0.120 8 134599702 non coding transcript exon variant A/C snv 0.11 1
rs1038025
TOMM40
1.000 0.080 19 44901715 3 prime UTR variant T/C;G snv 1
rs1038026
TOMM40
1.000 0.080 19 44901805 3 prime UTR variant A/G;T snv 4
rs10401176
BCL3
1.000 0.080 19 44750234 intron variant C/G;T snv 0.17 2
rs10402271 1.000 0.080 19 44825957 downstream gene variant T/G snv 0.28 7
rs10405693 1.000 0.080 19 44823407 downstream gene variant C/T snv 0.28 1
rs10407439 1.000 0.080 19 44838691 intergenic variant A/G snv 0.69 1
rs10408847
MARK4 ; PPP1R37
1.000 0.080 19 45131424 intron variant G/C snv 0.26 1
rs10412413 1.000 0.080 19 44824052 downstream gene variant C/T snv 0.30 1
rs10415983
MARK4 ; BLOC1S3
1.000 0.080 19 45208340 intron variant C/T snv 0.26 1
rs10416371
NKPD1 ; LOC105372420 ; MARK4
1.000 0.080 19 45156878 intron variant A/C;T snv 1
rs10421247
NKPD1 ; MARK4 ; LOC105372420
1.000 0.080 19 45154228 intron variant C/T snv 0.52 1