Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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 1
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
rs1038026
TOMM40
1.000 0.080 19 44901805 3 prime UTR variant A/G;T snv 3
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 4
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
rs10421247
NKPD1 ; MARK4 ; LOC105372420
1.000 0.080 19 45154228 intron variant C/T snv 0.52 1
rs10426401
LOC107985305 ; PVR
1.000 0.080 19 44644419 intron variant T/G snv 0.32 2
rs10455152 1.000 0.080 6 85308630 intergenic variant A/C snv 0.29 1
rs1049296
TF
0.882 0.120 3 133775510 missense variant C/T snv 0.16 0.14 2
rs1049564
PNP
0.882 0.160 14 20472447 missense variant G/A snv 0.19 0.21 2
rs10498633
SLC24A4
0.925 0.080 14 92460608 intron variant G/T snv 0.19 1
rs10501320
MADD ; MADD-AS1
0.925 0.120 11 47272248 5 prime UTR variant G/C snv 0.17 5
rs1051338
LIPA
0.807 0.120 10 89247603 missense variant T/G snv 0.32 0.26 1
rs1060743
BIN1
0.925 0.080 2 127068957 synonymous variant A/G snv 0.34 0.29 1
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 5