Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4129585
TSNARE1 ; LOC107986983
1.000 0.040 8 142231572 intron variant A/C snv 0.68 4
rs4356203
PIK3C2A
0.925 0.040 11 17138601 intron variant A/G snv 0.31 4
rs4870888
FER1L6 ; FER1L6-AS2
0.882 0.040 8 124096736 intron variant T/C snv 0.39 4
rs506597 0.882 0.040 7 100715797 upstream gene variant A/G snv 0.90 4
rs62173322
KLHL23
0.882 0.040 2 169754519 intron variant A/G snv 0.32 4
rs6586354 0.851 0.040 1 234897489 intron variant G/A snv 0.25 4
rs6704768
GIGYF2
1.000 0.040 2 232727791 intron variant G/A snv 0.54 4
rs6855246 1.000 0.040 4 102191313 intergenic variant A/G snv 0.14 4
rs7219021
TTLL6
0.925 0.040 17 48763179 intron variant T/G snv 0.26 4
rs76371172
OTUD7A ; LOC105370753
0.882 0.040 15 31522252 intron variant T/G snv 9.1E-03 4
rs7872515
SPTLC1
0.925 0.040 9 92060258 intron variant G/A snv 0.25 4
rs9577511
GRTP1
0.882 0.040 13 113337508 intron variant A/G snv 0.15 4
rs9862857
LOC101927995 ; LOC105377013
0.851 0.040 3 30453840 regulatory region variant A/G;T snv 4
rs1042779
ITIH1
0.882 0.040 3 52786995 missense variant A/G snv 0.40 0.42 3
rs105633
DELE1 ; PCDH12
0.882 0.040 5 141945684 synonymous variant T/C;G snv 0.98; 4.0E-06 3
rs10752262
CAMK1D
1.000 0.040 10 12353101 intron variant C/T snv 0.39 3
rs10774037
CACNA1C
0.882 0.040 12 2311360 intron variant G/A snv 0.77 3
rs11055980
ATF7IP
1.000 0.040 12 14458588 intron variant C/T snv 0.40 3
rs11125080
ATP6V1E2
0.882 0.040 2 46505266 intron variant G/A;C snv 3
rs11210892 1.000 0.040 1 43634413 intergenic variant G/A snv 0.51 3
rs115777110
LOC107985255
0.882 0.040 1 208936211 intergenic variant T/C snv 1.2E-02 3
rs11688767
ACTG1P22
0.925 0.040 2 57761059 intron variant A/T snv 0.40 3
rs11740474
GALNT10
1.000 0.040 5 154301187 intron variant A/T snv 0.37 3
rs11765189
PTPRN2
1.000 0.040 7 157743285 intron variant A/G snv 0.25 3
rs12052005
CCDC102B
0.882 0.040 18 68832311 intron variant G/C;T snv 3