Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs780571007
EFHC1
1.000 0.040 6 52454113 missense variant A/G snv 3.2E-05 5.6E-05 1
rs377286138
EFHC1
1.000 0.040 6 52479064 missense variant C/T snv 1.1E-04 7.0E-05 1
rs781665913
EFHC1
1.000 0.040 6 52452688 missense variant G/A snv 6.4E-05 8.4E-05 1
rs142458862
EFHC1
1.000 0.040 6 52492274 missense variant T/G snv 1.8E-04 1.2E-04 1
rs527295360
EFHC1
1.000 0.040 6 52465035 missense variant C/T snv 2.1E-04 1.5E-04 1
rs371151471
EFHC1
1.000 0.040 6 52465092 missense variant C/T snv 1.2E-03 2.0E-04 1
rs121918817
SCN1A-AS1 ; SCN1A
0.882 0.040 2 166045080 missense variant C/T snv 1.7E-03 1.5E-03 3
rs137852776
EFHC1
0.827 0.080 6 52452799 missense variant T/C snv 3.5E-03 2.4E-03 5
rs79761183
EFHC1
0.925 0.040 6 52452776 missense variant G/A;C snv 2.0E-03; 8.0E-06; 1.2E-05 7.6E-03 2
rs149055334
EFHC1
0.925 0.040 6 52424111 missense variant C/A snv 1.9E-03 7.7E-03 2
rs1570624
EFHC1
0.882 0.040 6 52454252 missense variant G/A snv 1.0E-02 9.6E-03 3
rs1799963
F2
0.695 0.400 11 46739505 3 prime UTR variant G/A snv 9.6E-03 25
rs17851770
EFHC1
1.000 0.040 6 52492273 missense variant A/C snv 6.2E-02 6.2E-02 1
rs3918149
BRD2 ; HLA-DMA
1.000 0.040 6 32968596 5 prime UTR variant G/A snv 0.11 1
rs10496964 0.925 0.040 2 144602342 intergenic variant C/T snv 0.12 2
rs4906902
GABRB3
0.724 0.200 15 26774621 intron variant A/G snv 0.15 14
rs12059546
CHRM3
0.925 0.040 1 239806797 intron variant A/G snv 0.30 2
rs3743123
GJD2
1.000 0.040 15 34752856 synonymous variant G/A snv 0.32 0.31 1
rs211037
GABRG2
0.742 0.240 5 162101274 synonymous variant C/T snv 0.28 0.31 14
rs2029461
GRM4
1.000 0.040 6 34138013 intron variant C/T snv 0.43 1
rs1046276
CTF1
1.000 0.040 16 30903305 3 prime UTR variant T/C snv 0.62 3