Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs547643
ABO
9 133259656 intron variant C/T snv 0.27 3
rs549331
ABO
9 133259791 intron variant C/G snv 0.28 3
rs549446
ABO
9 133259834 missense variant C/T snv 0.27 3
rs574347
ABO
9 133260255 intron variant T/C snv 0.27 3
rs579483
ABO
9 133260793 intron variant T/A snv 3
rs579622
ABO
9 133260839 intron variant G/A snv 3
rs613423
ABO
9 133260074 intron variant G/A snv 0.27 3
rs61871700
CPN1
10 100068504 intron variant C/A;T snv 3
rs624601
ABO
9 133259961 intron variant G/A snv 0.28 3
rs6498142
CLEC16A
16 10987392 intron variant C/G snv 0.77 3
rs688976
ABO
9 133261367 missense variant C/A snv 3
rs7078003
HOGA1
10 97599655 non coding transcript exon variant C/T snv 0.14 0.14 3
rs7940310
PAFAH1B2
11 117153765 intron variant T/A;C snv 3
rs8176717
ABO
9 133257647 intron variant G/T snv 0.26 3
rs8176728
ABO
9 133257174 intron variant G/C;T snv 3
rs8176732
ABO
9 133256916 intron variant A/G snv 0.25 3
rs878521 7 44216044 downstream gene variant G/A snv 0.33 3
rs9637599
PPM1K ; PPM1K-DT
4 88285078 intron variant A/C snv 0.56 3
rs10083777
LOC107984858 ; CENPN
16 81031677 intron variant C/T snv 0.15 2
rs10146637
FBXO34
14 55278092 intron variant G/A snv 0.30 2
rs140348140
KIAA2026
9 5877295 downstream gene variant -/A delins 3.1E-02 2
rs1562064 4 145391948 intergenic variant G/A snv 0.74 2
rs17159338
LINC01950
5 106942471 intron variant T/C snv 6.8E-02 2
rs1718309
PAH
12 102848618 intron variant A/G snv 0.67 2
rs172642
C17orf100 ; SLC13A5 ; ALOX15P1
17 6692079 intron variant A/C snv 0.64 2