Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10015639
AFF1
4 86970413 intron variant A/G snv 0.76 1
rs10023020
EXOSC9
4 121803449 intron variant G/A snv 0.30 1
rs10023050 4 87143279 downstream gene variant A/G snv 0.34 1
rs10023056 4 87143314 downstream gene variant A/G snv 0.19 1
rs10032244
AFF1
4 86996779 intron variant A/G snv 0.63 1
rs1003688
SCGN
6 25658944 intron variant G/A snv 0.14 2
rs1006081
CCDC162P
6 109304347 intron variant T/A;C snv 1
rs1007176 6 164070805 intergenic variant A/G snv 0.55 1
rs1008084
CCDC162P
6 109305762 intron variant G/A snv 0.40 2
rs10080880
LOC101928277
6 134868890 intergenic variant G/A snv 0.14 1
rs10084948
BBS7
4 121844494 intron variant C/T snv 0.30 1
rs10086987 1.000 0.040 8 47177908 intron variant G/A;C snv 1
rs1009082
SPECC1
17 20159646 intron variant G/A snv 0.24 1
rs10099197
LOC105379392 ; ANK1
8 41796940 intron variant C/T snv 0.79 1
rs1010222
CALR
19 12937794 upstream gene variant A/G snv 0.70 3
rs1010549 6 164071351 intergenic variant A/C snv 0.50 1
rs1010902
C4orf36
4 86898002 intron variant C/T snv 0.14 1
rs1010903
C4orf36
4 86898040 intron variant C/T snv 0.14 1
rs10109400 8 42600210 intergenic variant T/C snv 0.66 1
rs1012898
CARMIL1
6 25604487 intron variant G/A snv 0.40 1
rs1013891
MYB ; LOC105378011
6 135217501 intron variant A/G;T snv 1
rs1014021
HBS1L
6 135013462 intron variant A/G snv 0.53 1
rs1015149
TFEB
6 41691151 synonymous variant C/T snv 0.46 0.50 1
rs1015150
TFEB
6 41691566 intron variant C/T snv 0.47 1
rs1015670
DOT1L
19 2171491 intron variant G/A snv 0.46 1