Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs111611512 Y 11313671 upstream gene variant T/A;C;G snv 1
rs111705907
ARHGEF6
X 136761844 intron variant A/G snv 1.1E-02 1
rs5916200 X 5673774 intron variant A/G snv 1
rs5917854 X 39625866 intergenic variant C/T snv 0.39 1
rs5952155 X 116371826 intergenic variant A/T snv 1
rs61355905
FGF13
X 139213616 intron variant C/T snv 4.2E-02 1
rs7053320
MID1
X 10573070 intron variant C/T snv 0.12 1
rs7061829 X 118188982 regulatory region variant G/C snv 1.2E-02 1
rs12483959
PNPLA3
1.000 22 43930116 intron variant G/A;C;T snv 4
rs2040771 22 19174422 downstream gene variant C/A;T snv 3
rs712964 22 19168604 upstream gene variant T/C snv 0.66 2
rs1018764
CLTCL1
22 19184493 3 prime UTR variant T/C snv 0.75 0.75 1
rs1061325
LOC112268289 ; CLTCL1
22 19196584 missense variant T/C snv 0.49 0.43 1
rs1091013
CLTCL1
22 19261064 intron variant C/G;T snv 1
rs11089258 22 19174763 downstream gene variant C/T snv 0.40 1
rs11089259
CLTCL1
22 19202633 intron variant C/G;T snv 1
rs1206544
CLTCL1
22 19227516 intron variant C/T snv 0.62 1
rs12485084 22 19174813 downstream gene variant A/G snv 0.37 1
rs1340958
CLTCL1
22 19265809 intron variant A/C;G snv 1
rs1771540
CLTCL1
22 19186421 intron variant T/A snv 0.75 1
rs1780637
CLTCL1
22 19190738 intron variant A/C;G snv 1
rs1780639
CLTCL1
22 19187091 intron variant T/A;C snv 1
rs1780640
CLTCL1
22 19187085 intron variant C/G;T snv 1
rs1780642
CLTCL1
22 19183091 non coding transcript exon variant T/A;C snv 1
rs1780643
CLTCL1
22 19204215 intron variant T/C snv 0.75 1