Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11220463
ST3GAL4
11 126378316 intron variant A/T snv 0.12 3
rs1169310
C12orf43 ; HNF1A
12 121001630 3 prime UTR variant G/A snv 0.31 3
rs12034383
CR1
1 207630250 intron variant G/A snv 0.47 3
rs12741825 1 159700355 downstream gene variant C/T snv 0.24 3
rs12753193 1 65703996 non coding transcript exon variant G/A snv 0.58 3
rs1688043
HPN-AS1 ; HPN
19 35062437 intron variant C/G;T snv 3
rs1936797 6 127111512 intron variant A/G snv 0.33 3
rs1998303 9 82800066 intergenic variant A/G snv 0.37 3
rs2710804 7 36044919 intron variant T/C snv 0.29 3
rs3027012
CADM3-AS1 ; ACKR1
1 159204333 5 prime UTR variant C/T snv 0.13 3
rs3213545
OASL
12 121033534 synonymous variant G/A snv 0.32 0.26 3
rs340005
RORA-AS1 ; RORA
15 60585831 intron variant G/A snv 0.67 3
rs340025
RORA ; RORA-AS1
15 60616108 intron variant T/A;C snv 3
rs3822857
FRK
6 115992768 intron variant G/A;C snv 3
rs4660808
PPIEL
1 39552837 intron variant C/T snv 0.17 3
rs4703642
LOC105379040
5 74966337 intron variant A/G snv 0.50 3
rs4910742
HBG2 ; HBE1
11 5285279 intron variant G/A;T snv 3
rs661955 1 234707109 upstream gene variant G/C;T snv 3
rs7012637 8 9315699 intron variant G/A;C snv 3
rs7621025
STAG1
3 136553404 intron variant T/A;C snv 3
rs8180991 8 125488108 intron variant C/G snv 0.19 3
rs10255299
DOCK4
7 111887504 intron variant G/A snv 0.11 2
rs10435719 8 11919395 downstream gene variant C/T snv 0.48 2
rs10744775
BRAP
12 111658411 intron variant T/C snv 0.44 2
rs10778215
C12orf42
12 103143488 intron variant T/A;G snv 2