Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10894993 0.925 0.080 11 100627998 intergenic variant T/G snv 4.7E-02 2
rs11763020
C7orf50
1.000 0.040 7 1020652 intron variant C/T snv 0.12 1
rs4684677
GHRLOS ; GHRL
0.742 0.360 3 10286769 missense variant T/A snv 0.10 6.6E-02 13
rs4145262 1.000 0.040 12 105659532 regulatory region variant C/A snv 4.8E-02 1
rs1326656542
LIG4
0.776 0.280 13 108210293 missense variant A/T snv 4.0E-06 10
rs12061304
LOC107985174
1.000 0.040 1 110695063 intergenic variant A/G snv 0.30 1
rs17260539 1.000 0.040 9 12182545 intergenic variant G/A snv 6.6E-02 1
rs7309727
TMEM132D
1.000 0.040 12 129470814 intron variant T/C snv 0.75 1
rs11060369
TMEM132D
1.000 0.040 12 129475652 intron variant A/C snv 0.41 1
rs13356494 1.000 0.040 5 135991866 regulatory region variant C/G;T snv 1
rs10216809
SGCZ
0.925 0.080 8 14507414 intron variant C/G;T snv 2
rs144783209
SMAD1
1.000 0.040 4 145482377 intron variant G/C;T snv 1
rs9372078 1.000 0.040 6 150592825 intergenic variant T/A snv 0.73 1
rs3213207
DTNBP1
0.776 0.120 6 15627871 intron variant T/C snv 8.7E-02 11
rs7688285 0.925 0.040 4 157047466 intergenic variant G/A snv 0.10 2
rs191260602
GLRB
1.000 0.040 4 157140489 intron variant A/G snv 7.7E-03 1
rs17035816
GLRB
0.925 0.040 4 157167312 intron variant A/G snv 0.11 2
rs3219151
GABRA6
0.752 0.160 5 161701908 3 prime UTR variant C/T snv 0.51 14
rs11724320
NPY5R ; NPY1R
0.925 0.040 4 163346771 intron variant T/C snv 0.56 2
rs11946004
NPY5R
0.925 0.040 4 163351551 synonymous variant G/A;T snv 0.10; 4.0E-06 2
rs3749034
GAD1
0.827 0.040 2 170816965 5 prime UTR variant G/A;T snv 6
rs2241165
GAD1
1.000 0.040 2 170821869 non coding transcript exon variant C/T snv 0.63 1
rs8076112
TLCD2
1.000 0.040 17 1708905 intron variant A/C;G snv 0.15 1
rs6502892
MIR22 ; MIR22HG
1.000 0.040 17 1714314 intron variant T/C;G snv 1
rs1800532
TPH1
0.763 0.160 11 18026269 intron variant G/T snv 0.33 15