Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397933924 10 97314229 upstream gene variant -/CAGGTTCAAGCGA ins 5
rs12357266
LOC105378447 ; ARHGAP19-SLIT1
10 97218288 intron variant G/A snv 0.51 2
rs2072910
PLCB4
20 9384656 intron variant T/C snv 0.23 1
rs445
CDK6
7 92779056 intron variant C/T snv 0.14 9
rs3742716
RIN3
14 92652324 synonymous variant G/A snv 0.32 0.25 2
rs72699866
RIN3
14 92648442 intron variant G/A snv 0.14 4
rs8179
CDK6
0.882 0.080 7 92606850 3 prime UTR variant T/A;C;G snv 5
rs2246941
LIPA
10 89245159 intron variant C/A;T snv 2
rs12752838 1 8853597 upstream gene variant A/G snv 0.54 4
rs10858740 12 88451258 intergenic variant A/G;T snv 0.56 5
rs11104881 12 88449697 intergenic variant T/A;C snv 1
rs7587928
KIDINS220
2 8808940 intron variant T/C snv 0.29 1
rs200638392 6 87128241 intergenic variant GAT/-;GATGAT delins 0.47 5
rs9926664
IRF8
16 85905149 intron variant A/G snv 0.19 2
rs305082
IRF8
16 85903372 non coding transcript exon variant T/C snv 0.28 3
rs28476539
SCD5
4 82631138 3 prime UTR variant G/A;T snv 3
rs272594 8 80557885 upstream gene variant A/C snv 0.22 1
rs7804306
GLCCI1
7 7978549 intron variant G/A snv 0.11 4
rs377079849
NAA38 ; CHD3
17 7884458 intron variant ATATATATATAT/-;AT;ATAT;ATATAT;ATATATAT;ATATATATAT;ATATATATATATAT;ATATATATATATATAT;ATATATATATATATATAT;ATATATATATATATATATAT;ATATATATATATATATATATAT;ATATATATATATATATATATATAT;ATATATATATATATATATATATATAT;ATATATATATATATATATATATATATAT;ATATATATATATATATATATATATATATAT delins 0.46 3
rs1968252
LOC105372263
19 7782850 upstream gene variant G/A;T snv 5
rs4804815
LOC105372263
19 7777783 intergenic variant C/G snv 0.19 1
rs11625487
ISM2
14 77495266 intron variant G/A;C snv 0.70 2
rs11361923
NOXRED1
14 77396337 intron variant C/- delins 0.54 4
rs749780
RAB37 ; CD300LF
17 74703245 intron variant C/A snv 0.54 4
rs549280 4 74105479 intergenic variant G/A snv 0.57 2