Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12444979
LOC105371116
1.000 0.080 16 19922278 intergenic variant C/T snv 0.11 4
rs12463617 1.000 0.080 2 629244 regulatory region variant A/C;T snv 4
rs12955983 1.000 0.080 18 60205756 intergenic variant A/G snv 0.20 4
rs12969709 1.000 0.080 18 60192330 upstream gene variant C/A snv 0.21 4
rs1330
NUCB2
1.000 0.080 11 17294482 intron variant C/T snv 0.30 4
rs1514175
TNNI3K ; LRRC53 ; FPGT-TNNI3K
1.000 0.080 1 74525960 intron variant A/G snv 0.48 4
rs17700144 1.000 0.080 18 60144750 intron variant G/A snv 0.14 4
rs2207139 1.000 0.080 6 50877777 intergenic variant A/G snv 0.16 4
rs4771122
MTIF3
1.000 0.080 13 27446043 intron variant G/A;C snv 4
rs4929949
STK33
1.000 0.080 11 8583046 intron variant T/C snv 0.46 4
rs62033400
FTO
1.000 0.080 16 53777876 intron variant A/G snv 0.30 4
rs7132908
FAIM2
1.000 0.080 12 49869365 3 prime UTR variant G/A snv 0.31 4
rs939583 1.000 0.080 2 622531 intergenic variant C/T snv 0.85 4
rs9939973
FTO
1.000 0.080 16 53766656 intron variant G/A snv 0.42 4
rs10182181 1.000 0.080 2 24927427 intergenic variant A/G snv 0.57 3
rs10835211
BDNF ; BDNF-AS
1.000 0.080 11 27679818 intron variant G/A snv 0.19 3
rs11042023
TRIM66
1.000 0.080 11 8640969 missense variant T/C snv 0.60 0.59 3
rs11075985
FTO
1.000 0.080 16 53771295 intron variant C/A snv 0.42 3
rs11624704
NRXN3
1.000 0.080 14 78319734 intron variant A/C snv 0.13 3
rs1457489 1.000 0.080 18 60194728 upstream gene variant G/A snv 0.29 3
rs1553548194
SCN1A-AS1 ; SCN1A
1.000 0.080 2 166048938 inframe deletion AAT/- delins 3
rs17381664
ZZZ3
1.000 0.080 1 77582646 intron variant T/C snv 0.29 3
rs17817288
FTO
1.000 0.080 16 53773852 intron variant A/C;G snv 3
rs1993709
LOC105378797
1.000 0.080 1 72372846 intron variant A/G snv 0.85 3
rs2272127
IL18RAP
1.000 0.080 2 102423413 intron variant C/G snv 0.22 3