Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1275805226
AGT
0.776 0.240 1 230706148 frameshift variant G/- del 7.0E-06 12
rs2059806
INSR
0.807 0.240 19 7166365 synonymous variant C/G;T snv 4.0E-06; 0.26 7
rs1341667
STOX1
0.925 0.040 10 68882104 missense variant T/C snv 0.62 0.57 4
rs7576192 1.000 0.040 2 120360455 intergenic variant A/G snv 0.68 2
rs7579169 1.000 0.040 2 120360548 intergenic variant T/C snv 0.68 2
rs2507800
ANGPT1
1.000 0.040 8 107250441 3 prime UTR variant T/A snv 0.36 2
rs3756261
EGF
0.925 0.160 4 109911150 upstream gene variant T/C snv 9.9E-02 2
rs1800595
F5
0.925 0.080 1 169541110 missense variant T/C;G snv 5.7E-02 2
rs770016471
ACE
1.000 0.040 17 63497260 missense variant C/G snv 1.4E-05 1
rs2198532
DCDC2C
1.000 0.040 2 3827777 intron variant T/C snv 0.79 1
rs779370907
ISYNA1
1.000 0.040 19 18436405 synonymous variant C/T snv 6.0E-05 1.4E-05 1
rs780972489
ISYNA1
1.000 0.040 19 18436831 synonymous variant C/T snv 8.9E-06 7.0E-06 1
rs7020782
PAPPA
1.000 0.040 9 116344602 missense variant C/A snv 0.68 0.59 1