Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1557043622
SLC35A2
0.695 0.400 X 48909843 missense variant C/A snv 46
rs757075712
TFAM
0.763 0.200 10 58390856 missense variant C/T snv 1.6E-05 1.4E-05 15
rs211037
GABRG2
0.742 0.240 5 162101274 synonymous variant C/T snv 0.28 0.31 14
rs74315342
NPHS2
0.763 0.120 1 179561327 missense variant C/T snv 6.0E-04 5.3E-04 10
rs200482683
AXDND1 ; NPHS2
0.827 0.120 1 179552608 missense variant C/T snv 1.1E-04 1.1E-04 6
rs121908131
APTX
0.851 0.240 9 32984784 missense variant G/A snv 2.8E-05 7.0E-06 4
rs121908132
APTX
0.851 0.240 9 32974544 missense variant A/C snv 4
rs767419411
PPOX
0.882 0.200 1 161168069 missense variant G/A;C snv 1.2E-05; 8.0E-06 3
rs2290732
GABRA1
0.925 0.160 5 161897892 3 prime UTR variant A/G;T snv 2