Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7914558
CNNM2
0.851 0.040 10 103016151 intron variant G/A snv 0.40 5
rs9297357
ZFPM2 ; LOC105375695
0.851 0.040 8 105130105 intron variant C/G;T snv 5
rs9951150 0.851 0.040 18 55153893 intergenic variant A/G;T snv 5
rs10405744
ZNF93
0.851 0.040 19 19948684 intron variant G/A snv 9.0E-02 4
rs1054442
DDN
0.925 0.040 12 48995537 3 prime UTR variant A/C snv 0.46 4
rs10968749
LINGO2
0.851 0.040 9 28752486 intergenic variant A/G snv 5.5E-02 4
rs11004733
PCDH15
0.882 0.040 10 55089584 intron variant C/T snv 2.9E-02 4
rs11829119
LOC107984527
0.851 0.040 12 19040597 intergenic variant T/A;C snv 4
rs141252918
CCDC170
0.882 0.040 6 151506923 intron variant G/A;C snv 4
rs149268645
WDR12 ; CARF
0.882 0.040 2 202968295 intron variant G/A snv 8.4E-02 4
rs16875288
ADAMTS16 ; LOC101929200
0.851 0.040 5 5297087 intron variant A/T snv 0.22 4
rs16935279
LINC01592
0.851 0.040 8 68961217 intron variant T/C snv 1.9E-02 4
rs17066873 0.851 0.040 13 76889874 non coding transcript exon variant T/C snv 5.4E-02 4
rs17154917 0.851 0.040 7 81207393 intergenic variant G/A;T snv 4
rs17158930
DOCK4
0.851 0.040 7 111871082 intron variant A/G snv 0.25 4
rs17211233
RASGRF2
0.882 0.040 5 81072944 intron variant T/A;C snv 4
rs17673138
NRG1
0.851 0.040 8 32840440 intron variant A/C snv 8.6E-02 4
rs17746001 0.925 0.040 4 179734472 intergenic variant C/T snv 5.3E-02 4
rs17790731
RFESD
0.851 0.040 5 95647825 5 prime UTR variant C/T snv 4.9E-02 4
rs2054399
KCNMB2-AS1 ; KCNMB2
0.925 0.040 3 178623794 intron variant G/A;C snv 4
rs2287921
RASIP1
1.000 0.040 19 48725015 non coding transcript exon variant T/C snv 0.37 4
rs2302045
MTERF4 ; SNED1
0.851 0.040 2 241081801 splice region variant G/A snv 7.6E-02 1.0E-01 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