Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9806366 15 101262752 intergenic variant C/T snv 0.24 1
rs9972727 16 31137821 upstream gene variant A/C;G snv 1
rs7173826
AAGAB
15 67236036 missense variant T/C;G snv 8.0E-06; 0.37 1
rs144588452
ABCA1
9 104784371 missense variant C/T snv 2.2E-04 1.5E-04 1
rs35315125
ABCF3
3 184187521 non coding transcript exon variant G/C snv 1.5E-02 1
rs2627308
ABHD17C
15 80723086 intron variant C/A snv 0.33 1
rs765803965
ACE
17 63480345 missense variant G/A snv 4.0E-06 1
rs11647570
ADCY9
16 4087261 intron variant A/G snv 0.20 1
rs10824134
ADK
10 74261866 intron variant T/C snv 0.48 1
rs12363917
ALG9
11 111793677 intron variant C/G;T snv 1
rs1962094
ARMC4
10 27963710 intron variant T/A;C snv 1
rs6781726
ATG7
3 11467491 intron variant C/T snv 0.50 1
rs2356455
ATL1
14 50626424 intron variant G/A snv 0.48 1
rs12928131
AXIN1
16 292771 non coding transcript exon variant C/T snv 0.12 1
rs6565564
BAHCC1
17 81408117 intron variant G/C snv 0.96 1
rs13127398
BANK1
4 102000547 intron variant T/A snv 4.1E-02 1
rs3785837
BCAS3
17 61391581 non coding transcript exon variant G/A snv 0.58 1
rs4948550
BICC1
10 58828793 missense variant T/C snv 0.71 0.64 1
rs2070325
BPIFB4
20 33086040 missense variant A/G snv 0.41 0.36 1
rs2205849
C1orf112 ; SELL
1 169712216 intron variant T/C snv 0.19 1
rs11601694
C1QTNF4
11 47593023 intron variant C/A;T snv 1
rs134557
C22orf31
22 29061594 intron variant A/G;T snv 0.84 1
rs6445597
CACNA1D
3 53700504 intron variant G/A snv 0.36 1
rs10740995
CACNB2
10 18156159 intron variant G/A;T snv 1
rs983521
CADPS2
7 122434362 intron variant A/G snv 0.27 1