Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs5756506
TMPRSS6
22 37071352 intron variant G/A;C snv 4
rs2238783
ARVCF
22 19984929 intron variant C/G snv 0.42 3
rs62237617
TTC28
22 28365160 intron variant C/G;T snv 1.9E-03 3
rs878825
YDJC
22 21627960 upstream gene variant T/C snv 0.32 3
rs9609565 22 32471541 upstream gene variant G/A snv 0.24 3
rs1977080
PNPLA3
22 43934151 intron variant C/T snv 0.19 2
rs4819618
BCL2L13
22 17651042 intron variant G/A;T snv 2
rs713909
CBX7
22 39136415 non coding transcript exon variant G/A;C;T snv 2
rs758374
ARVCF
22 19984029 intron variant T/C snv 0.27 2
rs9606618
TMEM121B
22 17116671 3 prime UTR variant G/A snv 4.5E-03 2
rs9611177 1.000 0.040 22 39444125 intergenic variant C/T snv 0.29 2
rs132644
APOL3
22 36149778 3 prime UTR variant T/C snv 0.84 0.69 1
rs138909
TSPO
22 43153733 intron variant T/A;C snv 1
rs139407 22 39156070 upstream gene variant G/A snv 0.45 1
rs143008696
IL17RA
22 17097075 missense variant C/T snv 1.8E-03 2.2E-03 1
rs1894474 22 29842085 upstream gene variant A/G snv 0.47 1
rs1997719
EMID1
22 29232752 non coding transcript exon variant C/A;T snv 1
rs2070904
CYP2D8P ; LOC105377203
22 42150456 intron variant T/C snv 0.47 1
rs2238754
DGCR2
22 19070633 intron variant C/T snv 6.5E-02 1
rs34505104
GGT5
22 24228641 intron variant A/G snv 0.32 1
rs369081
MICAL3
22 17803906 intron variant T/C snv 0.39 0.52 1
rs5760096 22 23905123 non coding transcript exon variant A/G snv 0.73 1
rs59667935
CECR2
22 17427131 intron variant A/C snv 0.15 1
rs926928
DRG1
22 31425733 intron variant G/A snv 0.46 1
rs2835731
DYRK1A
1.000 0.040 21 37424426 intron variant C/G;T snv 0.17 2