Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs112925537
INO80
15 41042015 intron variant -/C ins 2
rs567058829
TNN
1 175142624 intron variant -/A ins 1
rs78763922 4 143133400 intron variant AG/- del 0.27 2
rs137976953
C1orf167
1 11782952 intron variant T/- del 1.0E-01 1
rs5883070 7 27240226 intron variant -/AAAACA;AACA delins 0.91 5
rs10628234 15 74918801 downstream gene variant -/CA delins 2
rs201133964 8 8750340 intron variant GT/- delins 2
rs201851995
RSRC1
3 158119720 intron variant TTAT/- delins 1.4E-04 2
rs202071545
CLCN6
1 11818105 intron variant AAAA/-;AAA;AAAAA;AAAAAA delins 2
rs138475089 7 100899019 upstream gene variant -/TA delins 1
rs144449115
CEP83 ; PLXNC1
12 94298853 intron variant AAGA/- delins 4.6E-02 1
rs146669915
SOX6
11 16269264 intron variant -/CTGT delins 1
rs149364745
FBLN5
14 91925128 intron variant ATCAA/- delins 0.30 1
rs17875419 10 114037712 intergenic variant G/- delins 0.14 1
rs3063286
SLX4IP
20 10507905 intron variant TA/-;TATA;TATATA;TATATATA;TATATATATA delins 1
rs34846688
STAT3
17 42343456 intron variant TTTTTTTTTTTT/-;T;TT;TTT;TTTTT;TTTTTT;TTTTTTT;TTTTTTTT;TTTTTTTTT;TTTTTTTTTT;TTTTTTTTTTT;TTTTTTTTTTTTT;TTTTTTTTTTTTTT;TTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTT delins 0.30 1
rs35123175
HSF2BP
21 43586730 intron variant A/- delins 6.0E-02 1
rs35189230
DCBLD1
6 117495189 intron variant CA/-;CACA delins 1
rs35904419 8 9519301 intergenic variant T/-;TT;TTT delins 1
rs534298147
LOC105369686
12 20196697 intergenic variant T/-;TT;TTT;TTTT delins 1
rs535378844
NAA25
12 112073262 intron variant CACACACACA/-;CA;CACA;CACACA;CACACACA;CACACACACACA;CACACACACACACA;CACACACACACACACA;CACACACACACACACACA;CACACACACACACACACACA delins 6.3E-03 1
rs565853247 4 80247467 intergenic variant TT/-;T;TTT delins 1
rs571893049
SLC4A7
3 27449048 intron variant T/-;TT;TTT delins 1
rs60317590
LOC105370809
15 48651693 non coding transcript exon variant TTTTTTTTTTTT/-;TTTTTTT;TTTTTTTT;TTTTTTTTT;TTTTTTTTTT;TTTTTTTTTTT;TTTTTTTTTTTTT;TTTTTTTTTTTTTT;TTTTTTTTTTTTTTT delins 1
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 61