Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs34595852 9 86263457 upstream gene variant -/CT delins 0.75 2
rs35113840
ILKAP
2 238193015 intron variant -/A;AA delins 2
rs35219595
LOC107987100
9 94506901 intron variant G/- delins 0.69 2
rs35671561 1 205125419 upstream gene variant TTTTTTTTTTTTTT/-;TT;TTTTT;TTTTTTTTTT;TTTTTTTTTTT;TTTTTTTTTTTT;TTTTTTTTTTTTT;TTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTT delins 2
rs369837642
NT5C3A
7 33045761 intron variant TT/-;T;TTT delins 0.36 2
rs373214016
HAMP
19 35284607 non coding transcript exon variant T/-;TT;TTT delins 2
rs398051584 3 12230419 regulatory region variant T/-;TT;TTT;TTTTTTTTTTT delins 2
rs530424960
HBS1L
6 135028265 intron variant AAA/-;AA;AAAA;AAAAA delins 2
rs548688766
UBXN2A
2 23973640 intron variant T/-;TT;TTT delins 2
rs559546873
NT5C2
10 103186913 intron variant AAAA/-;A;AA;AAA;AAAAA;AAAAAA delins 0.33 2
rs566629828
SMIM1
1 3775434 frameshift variant AGCCTAGGGGCTGTGTC/- delins 9.2E-03 2
rs57236717
WDR20
14 102148541 intron variant AAA/-;A;AA;AAAA;AAAAA;AAAAAA;AAAAAAAAAA delins 2
rs577887768
DNAJC13
3 132487560 intron variant TTTTTTT/-;T;TTTTT;TTTTTT;TTTTTTTT;TTTTTTTTT;TTTTTTTTTT;TTTTTTTTTTT;TTTTTTTTTTTT;TTTTTTTTTTTTT;TTTTTTTTTTTTTT;TTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTT delins 2
rs5876027
CD2AP
6 47570142 intron variant TT/-;T;TTT;TTTT delins 2
rs67796445
LOC105371749
17 36483818 upstream gene variant G/-;GG;GGG delins 2
rs67806247
TMEM259
19 1014539 intron variant TGATGGGGCG/-;TGATGGGGCGTGATGGGGCG delins 2
rs71086466
DIP2B
12 50657224 intron variant AAAAAAAAAA/-;AA;AAA;AAAA;AAAAA;AAAAAA;AAAAAAAA;AAAAAAAAA;AAAAAAAAAAA;AAAAAAAAAAAA;AAAAAAAAAAAAA;AAAAAAAAAAAAAA;AAAAAAAAAAAAAAA;AAAAAAAAAAAAAAAAAAAAAAAAA;AAAAAAAAAAAAAAAAAAAAAAAAAAAA delins 0.36 2
rs71138029
HEATR3
16 50074982 non coding transcript exon variant AAA/-;AAAA;AAAAA;AAAAAA;AAAAAAAAAAAA delins 2
rs75926215 17 73180386 intron variant TTTT/-;T;TT;TTT;TTTTT;TTTTTT delins 0.32 2
rs79237498
RAC1
7 6397234 intron variant -/T;TT delins 2
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 55
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 35
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 30
rs429358
APOE
0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 26
rs7412
APOE
0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 20