Source: CLINVAR

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs778139192
KIF7 ; TICRR
0.776 0.360 15 89629561 stop gained G/A;T snv 4.1E-06; 7.3E-05 14
rs11575937
LMNA
0.653 0.480 1 156136985 missense variant G/A;T snv 14
rs6471
CYP21A2
0.683 0.360 6 32040110 missense variant G/A;C;T snv 1.2E-05; 5.3E-03 4
rs1805192
PPARG
0.510 0.840 3 12379739 missense variant C/G snv 4
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 3
rs854560
PON1
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 3
rs34911341
GHRL ; GHRLOS
0.882 0.200 3 10289835 missense variant C/T snv 7.0E-03 7.3E-03 2
rs696217
GHRL ; GHRLOS
0.662 0.640 3 10289773 missense variant G/T snv 8.8E-02 7.1E-02 2
rs1801278
IRS1
0.637 0.560 2 226795828 missense variant C/G;T snv 4.0E-06; 5.2E-02 2
rs1799724
LTA ; TNF
0.600 0.680 6 31574705 upstream gene variant C/T snv 8.5E-02 2
rs4994
ADRB3
0.578 0.640 8 37966280 missense variant A/G snv 0.11 9.2E-02 1
rs3792267
CAPN10
0.882 0.200 2 240591757 non coding transcript exon variant G/A snv 0.23 1
rs3842570
CAPN10
0.925 0.160 2 240594824 intron variant -/CGGGAGGAGGGTGATGATTCTGTCCCAGGAGC delins 1
rs5030952
CAPN10
0.925 0.160 2 240603286 intron variant C/G;T snv 1
rs1421085
FTO
0.752 0.280 16 53767042 intron variant T/C snv 0.31 1
rs1805097
IRS2
0.689 0.360 13 109782884 missense variant C/G;T snv 0.35 1
rs1051931
PLA2G7
0.708 0.400 6 46705206 missense variant A/G snv 0.81 0.79 1
rs6256
PTH
0.827 0.160 11 13492506 stop gained G/A;T snv 4.0E-06; 0.16 1
rs13266634
SLC30A8 ; LOC105375716
0.724 0.480 8 117172544 missense variant C/A;T snv 0.29 1
rs12255372
TCF7L2
0.667 0.480 10 113049143 intron variant G/A;T snv 1
rs2010963
VEGFA
0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 1