Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs78314028
CYTH3
1.000 0.040 7 6163445 3 prime UTR variant C/A snv 2.2E-02 3
rs7965830
LOC105369844
1.000 0.040 12 75962050 intron variant C/A;T snv 3
rs79661299 1.000 0.040 6 42088268 downstream gene variant C/G;T snv 3
rs8105292
LINC01782
1.000 0.040 19 32103916 non coding transcript exon variant T/C snv 0.19 3
rs9470398
CPNE5
1.000 0.040 6 36799290 intron variant T/C snv 5.5E-02 3
rs10519210 1.000 0.040 15 63445726 intergenic variant T/C;G snv 1
rs11172782 1.000 0.040 12 58865846 intergenic variant A/G snv 0.12 1
rs12638540
CMTM7
1.000 0.040 3 32447042 intron variant A/G;T snv 1
rs1520832 1.000 0.040 12 42859612 regulatory region variant T/C;G snv 1
rs2125623
OTUD7A
1.000 0.040 15 31537504 intron variant C/T snv 0.33 1
rs2210327
ADAMTSL1
1.000 0.040 9 18109237 intron variant A/T snv 3.4E-02 1
rs4528684 1.000 0.040 19 14240762 intergenic variant C/T snv 0.12 1
rs548097 1.000 0.040 13 75202132 intergenic variant G/C;T snv 1
rs737337
DOCK6
0.925 0.040 19 11236817 synonymous variant T/C snv 0.15 0.20 6
rs198358
NPPA-AS1 ; CLCN6
0.925 0.040 1 11844019 3 prime UTR variant T/C snv 0.32 4
rs1028728
POSTN
0.925 0.040 13 37599679 upstream gene variant A/T snv 0.20 3
rs10927887
CLCNKA
0.925 0.040 1 16024780 missense variant A/C;G snv 0.55 3
rs1249958
PPP1R1A
0.925 0.040 12 54582053 missense variant C/T snv 2.7E-02 3
rs1303946678
CYP2D6 ; NDUFA6-DT
0.925 0.040 22 42126851 missense variant C/G snv 3
rs200536955
HSPB6 ; PROSER3
0.925 0.040 19 35756980 missense variant G/A;T snv 7.0E-04 3
rs3829365
POSTN
0.925 0.040 13 37598759 5 prime UTR variant G/A;C snv 4.0E-06; 0.11 3
rs6026584
GNAS
0.925 0.040 20 58894018 intron variant T/C snv 0.70 3
rs10932374
ERBB4
0.925 0.040 2 211379678 3 prime UTR variant G/A snv 0.23 2
rs13003941
ERBB4
0.925 0.040 2 211378978 3 prime UTR variant G/C;T snv 0.26 2
rs1337916669
LOC108783645 ; HFE
0.925 0.040 6 26092879 missense variant G/T snv 2