Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2395792
USP49
6 41884449 intron variant T/G snv 0.97 1
rs607203 6 139520516 intron variant T/C snv 0.91 2
rs651821
APOA5
0.851 0.360 11 116791863 5 prime UTR variant C/T snv 0.88 0.89 10
rs762679
MCM4
8 47972876 missense variant T/A snv 0.87 0.88 4
rs198833 6 26114280 downstream gene variant G/A snv 0.87 1
rs10420951 19 18526808 upstream gene variant C/G snv 0.81 2
rs2140875 7 129963039 intron variant A/G snv 0.80 2
rs1484878
SLC14A1 ; LOC105372093
18 45723869 non coding transcript exon variant C/T snv 0.78 1
rs35091702
RBPMS
8 30421955 intron variant GAAAAAA/- delins 0.78 2
rs1234598
SLC16A10
6 111208250 intron variant A/T snv 0.77 1
rs7529925
LINC01221
1 199038079 intron variant C/T snv 0.77 3
rs6584485 10 102177487 intergenic variant C/T snv 0.76 1
rs1434282
LINC01221
1 199041592 non coding transcript exon variant C/T snv 0.76 5
rs1317931 11 128044858 regulatory region variant A/G snv 0.76 1
rs1569419
PRDM16
1 3080038 intron variant T/C snv 0.73 5
rs4833111
FAM114A1
4 38946069 downstream gene variant T/C snv 0.72 1
rs11673346
FARSA
19 12922126 upstream gene variant T/C snv 0.70 2
rs206913
BACH2
6 90227175 intron variant C/A snv 0.70 1
rs9310736
THRB
3 24309320 intron variant A/G snv 0.69 3
rs12582170 12 53364047 intergenic variant A/G snv 0.69 1
rs66682515 3 196094159 intergenic variant TTTT/-;T;TT;TTT;TTTTT;TTTTTT;TTTTTTTTTTTTTTTTT delins 0.69 1
rs11315539
RAB11A ; LOC105370866
15 65805720 intron variant TTTTT/-;T;TT;TTT;TTTT;TTTTTT;TTTTTTTT delins 0.69 1
rs11301805
TNRC6B
22 40196077 intron variant TTT/-;T;TT;TTTT;TTTTTTTTT delins 0.68 1
rs11857609
LOC105370866 ; RAB11A
15 65802932 intron variant T/C snv 0.68 3
rs35110281
HSF2BP
21 43649066 intron variant T/A snv 0.66 1