Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10965246 9 22132699 downstream gene variant T/C snv 0.15 2
rs1203936 20 22611792 upstream gene variant G/C;T snv 2
rs12053049
SPC25
2 168910638 intron variant T/C snv 5.2E-02 2
rs12670403
LOC101927609 ; AHR
7 17269655 intron variant C/A snv 0.46 2
rs12712928 2 44964941 intron variant G/C snv 0.18 2
rs13391552
ALMS1
2 73591809 intron variant G/A;C snv 2
rs1349497
RAPGEF4-AS1
2 172727935 intron variant G/A;C snv 2
rs1447352 11 92989595 downstream gene variant G/A snv 0.55 2
rs2023634
DGCR9 ; DGCR5
22 18984937 intron variant A/G snv 7.9E-02 2
rs2087160
ENPEP
4 110413574 intron variant G/T snv 0.68 2
rs2216405 2 210752170 intergenic variant A/G snv 0.15 2
rs2403254
HPS5
11 18303599 intron variant C/G;T snv 2
rs2411884
KCNQ1
11 2714304 intron variant C/A;G snv 2
rs2518049
AKR1C3
10 5095844 intron variant A/G;T snv 2
rs2652822
LACTB ; RPS27L
15 63130573 3 prime UTR variant T/C snv 0.41 2
rs272889
SLC22A4 ; MIR3936HG
5 132329685 intron variant A/G snv 0.64 2
rs4329
ACE
17 63486097 intron variant A/C;G snv 2
rs4581570 13 27936575 intergenic variant T/A;C snv 2
rs494562 6 85407411 intergenic variant A/G snv 0.16 2
rs503279
FUT2 ; LOC105447645
19 48705753 3 prime UTR variant T/C snv 0.48 2
rs57884925
GLIS3
9 4285119 intron variant C/G;T snv 2
rs6499165
SLC7A6OS ; SLC7A6
16 68292297 non coding transcript exon variant A/C snv 0.80 2
rs6558295
GPAA1
8 144084619 intron variant C/G snv 8.1E-02 0.14 2
rs662138
SLC22A1
6 160143444 intron variant C/G snv 0.14 2
rs76185967
RPL35P6 ; PSD3
8 18774816 non coding transcript exon variant C/T snv 1.6E-02 2