Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7729395
PAM
1.000 0.080 5 102764872 intron variant C/T snv 3.1E-02 2
rs2732860
TMEM182
2 102781875 intron variant G/A snv 0.55 1
rs12257568
SH3PXD2A
10 103763117 intron variant C/T snv 0.38 1
rs12678719
ZFPM2
1.000 8 105503826 intron variant C/G snv 0.37 2
rs76090503
CNTN6
3 1088135 upstream gene variant G/A snv 6.3E-03 1
rs79076257 8 109232394 intergenic variant T/C snv 4.3E-02 1
rs12127701
MYBPHL
1 109295642 intron variant A/G snv 6.2E-02 4
rs16858828
PHLDB2
3 111911940 intron variant A/C snv 0.17 1
rs75013985
KCND3
1 111987808 intron variant A/G snv 6.6E-03 1
rs17446418
CAMK2D
4 113496850 intron variant T/A;G snv 1
rs76270203 12 113499191 intergenic variant A/C snv 2.5E-02 1
rs6489953 12 114326957 intergenic variant C/A;T snv 1
rs3825214
TBX5
0.851 0.080 12 114357638 intron variant G/A snv 0.77 8
rs7312625
TBX5
1.000 0.080 12 114362169 intron variant G/A snv 0.71 3
rs4767237
TBX5
12 114363008 intron variant A/G snv 0.71 1
rs7135659
TBX5
12 114363967 intron variant G/A;C snv 1
rs1895585
TBX5
12 114364333 intron variant A/G;T snv 1
rs3825215
TBX5
12 114367093 intron variant G/A;C snv 1
rs1895582
TBX5
12 114369230 intron variant G/A snv 0.70 2
rs1895595
LOC105369998
12 114419889 regulatory region variant A/G snv 0.15 1
rs6489973
LOC105370000
12 114718718 intron variant A/G snv 0.35 1
rs1896312 12 114908619 intergenic variant C/T snv 0.71 1
rs11067773 12 115790690 intron variant T/C snv 7.8E-02 1
rs3807989
CAV1
1.000 0.080 7 116546187 intron variant A/G snv 0.53 2
rs11773845
CAV1
0.925 0.120 7 116551247 intron variant C/A snv 0.53 4