Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs140348140
KIAA2026
9 5877295 downstream gene variant -/A delins 3.1E-02 2
rs4652
LGALS3
0.752 0.200 14 55138318 missense variant A/C snv 4.1E-06; 0.45 0.57 12
rs75885714
PLCL2
3 16901018 intron variant A/C snv 4.6E-02 7
rs641959
ABO
9 133258308 intron variant A/C snv 0.29 4
rs9637599
PPM1K ; PPM1K-DT
4 88285078 intron variant A/C snv 0.56 3
rs172642
C17orf100 ; SLC13A5 ; ALOX15P1
17 6692079 intron variant A/C snv 0.64 2
rs1880889
PDZRN4
12 41327433 intron variant A/C snv 0.91 2
rs669408 1 232383404 regulatory region variant A/C snv 0.52 2
rs10142448
ATG14
14 55371390 intron variant A/C snv 0.43 1
rs11851870
FBXO34
14 55349264 intron variant A/C snv 0.15 1
rs1952087
LOC107984708
14 55216493 intergenic variant A/C snv 0.57 1
rs2183085
RPSAP13 ; WDHD1
14 55005673 non coding transcript exon variant A/C snv 0.43 1
rs2880103
LOC105370509 ; FBXO34
14 55271114 intron variant A/C snv 0.30 1
rs3783650
ATG14
14 55382254 intron variant A/C snv 0.57 1
rs3825613
LGALS3
14 55126454 intron variant A/C snv 0.36 1
rs7142204
TBPL2
14 55441718 intron variant A/C snv 0.52 1
rs8003684
LOC107984664 ; TBPL2
14 55425320 intron variant A/C snv 0.29 1
rs8007944 14 55110098 intergenic variant A/C snv 0.57 1
rs8010013
TBPL2
14 55418110 intron variant A/C snv 0.39 1
rs8011834
DLGAP5
14 55159259 intron variant A/C snv 0.48 1
rs8014621
TBPL2
14 55440131 intron variant A/C snv 0.49 1
rs9323280
FBXO34
14 55334969 intron variant A/C snv 0.11 1
rs942317
KTN1-AS1
14 55557104 intron variant A/C snv 0.56 1
rs657152
ABO
0.882 0.200 9 133263862 intron variant A/C;T snv 22
rs1002054
MAPK1IP1L
14 55062195 intron variant A/C;T snv 1