Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs221798
GIGYF1
0.882 0.040 7 100689872 intron variant C/A;G snv 3
rs221774 0.851 0.080 7 100701361 upstream gene variant A/G;T snv 4
rs506597 0.882 0.040 7 100715797 upstream gene variant A/G snv 0.90 4
rs11191454
LOC107984265 ; BORCS7-ASMT ; AS3MT
0.776 0.160 10 102900247 intron variant A/G snv 7.9E-02 5
rs7914558
CNNM2
0.851 0.040 10 103016151 intron variant G/A snv 0.40 5
rs11191580
NT5C2
0.827 0.040 10 103146454 intron variant T/C snv 7.9E-02 12
rs6484218
CAND1.11 ; AMPD3
0.882 0.040 11 10369034 intron variant G/A snv 0.21 4
rs7337127 0.925 0.080 13 104623579 intergenic variant C/A;T snv 2
rs12669727
LHFPL3 ; LHFPL3-AS1
1.000 0.040 7 104776829 intron variant T/A;C snv 1
rs735931
ATP2B2
1.000 0.040 3 10483412 intron variant A/G snv 0.60 1
rs9297357
ZFPM2 ; LOC105375695
0.851 0.040 8 105130105 intron variant C/G;T snv 5
rs73188321 1.000 0.040 7 105407711 intergenic variant C/T snv 0.35 1
rs6738485
UXS1
0.882 0.040 2 106193504 intron variant C/T snv 0.36 3
rs111940429
LINC01789
0.925 0.080 2 107366232 intron variant C/A;T snv 2
rs12871532 0.851 0.040 13 108016199 intergenic variant T/C snv 0.46 5
rs3804640
CD47
1.000 0.040 3 108074862 intron variant A/G snv 0.39 1
rs17040430 1.000 0.040 12 108349043 regulatory region variant G/T snv 5.9E-02 1
rs1536057
FOXO3
1.000 0.040 6 108564420 intron variant C/T snv 0.30 1
rs56031956
ACTL7A
0.882 0.040 9 108863349 missense variant C/G snv 2.3E-02 2.2E-02 3
rs7959663
MYO1H
0.925 0.040 12 109446562 intron variant G/A;C snv 2
rs10884920
ADD3
1.000 0.040 10 110015049 intron variant A/G;T snv 1
rs121912734
ATP2A2
0.925 0.120 12 110339638 missense variant T/C snv 1
rs12833856 1.000 0.040 12 110824378 intergenic variant A/G snv 1.6E-02 1
rs6568686
TRAF3IP2-AS1
1.000 0.040 6 111551279 intron variant T/C snv 0.83 1
rs77867520 0.882 0.040 4 11186225 intergenic variant C/T snv 7.2E-02 3