Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs495225
GHSR
0.882 0.040 3 172448243 synonymous variant G/A;C;T snv 0.66 4
rs554073050
CCK
0.925 0.040 3 42263460 synonymous variant G/A snv 1.2E-05 7.0E-06 3
rs10070190 0.925 0.040 5 26866262 intergenic variant G/A snv 0.60 2
rs11174202
TAFA2
0.925 0.040 12 61858476 intron variant A/G snv 0.49 2
rs11783752 0.925 0.040 8 20192013 intergenic variant G/A;C snv 2
rs12504244 0.925 0.040 4 54619021 intergenic variant C/A;G;T snv 2
rs13338499
LOC101927837
0.925 0.040 16 67486220 intron variant A/G;T snv 2
rs1356639869
LOC107986777 ; NPY
1.000 0.040 7 24289527 missense variant C/A snv 2
rs2834070 0.925 0.040 21 33015144 intron variant G/T snv 0.24 2
rs4825476
GRIA3
0.925 0.040 X 123307628 intron variant G/A;C snv 2
rs4869317
LNPEP
1.000 0.040 5 96956300 intron variant T/A snv 0.22 2
rs75063949
CARMIL1
0.925 0.040 6 25590813 intron variant C/G snv 0.14 2
rs10096097
LEPROTL1 ; DCTN6
1.000 0.040 8 30169582 intron variant G/A snv 0.62 1
rs10747478 1.000 0.040 1 96435899 intergenic variant T/A;C;G snv 1
rs11179027
TPH2
1.000 0.040 12 71983532 intron variant G/C snv 0.26 1
rs117957029
LOC105370064
1.000 0.040 12 127200688 intron variant T/C snv 1.4E-02 1
rs1285957 1.000 0.040 7 141889478 downstream gene variant T/C snv 0.86 1
rs1298806501
ESR2
1.000 0.040 14 64227600 missense variant G/A snv 4.0E-06 1
rs13100344 1.000 0.040 3 94886263 intergenic variant T/A snv 0.40 1
rs13125782
SORCS2
1.000 0.040 4 7426539 intron variant T/A;C;G snv 1
rs145241704 1.000 0.040 7 141805287 upstream gene variant T/G snv 7.4E-02 1
rs200312312
LOC105379109
1.000 0.040 5 104666645 intron variant T/C snv 0.16 1
rs2008387
MGMT
1.000 0.040 10 129650500 intron variant G/A snv 0.36 1
rs2287348
ERLEC1 ; GPR75-ASB3 ; ASB3
1.000 0.040 2 53812676 intron variant C/A;T snv 1
rs2295193
SYNE1
1.000 0.040 6 152131959 intron variant G/A;C snv 1