Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs71636784
ZDHHC18
1.000 0.040 1 26842709 intron variant T/G snv 0.12 4
rs3747631
LOC105371692 ; LRRN2
1.000 0.040 1 204618441 missense variant G/A;C snv 4.0E-06; 0.20 3
rs10783018
LOC101928219 ; LINC02607
1 95782279 non coding transcript exon variant G/A snv 0.74 2
rs10789285 1.000 0.040 1 69322799 intergenic variant T/G snv 0.33 2
rs10922907 1 90727492 downstream gene variant A/G;T snv 2
rs11265191
OR10J1 ; OR10J4
1 159430569 intron variant C/G;T snv 2
rs11588857
LRRN2 ; LOC105371692
1 204617919 missense variant G/A;T snv 0.20; 8.0E-06 2
rs12028010 1 41298799 intron variant T/C snv 0.19 2
rs12069733 1.000 0.040 1 43475837 TF binding site variant G/A snv 0.37 2
rs1343775 1 41292321 intron variant A/G snv 0.17 2
rs17043393
ESRRG
1 216698070 intron variant A/G snv 0.13 2
rs1831539
LINC01358
1 59094665 intron variant T/C snv 0.41 2
rs2163503
ZRANB2-AS2
1 71335356 intron variant A/C snv 0.17 2
rs3101338
LOC105378797
1 72284670 intron variant C/A snv 0.82 2
rs3128341
NEGR1 ; LOC105378797
1 72284165 intron variant T/C snv 0.82 2
rs41314284
STUM
1 226602300 3 prime UTR variant C/T snv 6.4E-02 2
rs589249
LOC105378648 ; LOC107984941
1.000 0.040 1 36696751 intergenic variant A/G;T snv 2
rs863006
CADM3-AS1
1 159207958 non coding transcript exon variant G/A snv 0.56 2
rs1037144 1 159598058 upstream gene variant G/A snv 0.51 1
rs1073090 1 96023656 downstream gene variant G/A snv 0.17 1
rs10783100
SNX7
1 98710740 intron variant T/G snv 0.51 1
rs10789442
KDM4A
1 43674404 intron variant A/C;G snv 1
rs10800624
LINC02789
1 199322594 intron variant C/T snv 0.20 1
rs10803130
SDCCAG8
1 243258102 intron variant A/G snv 0.43 1
rs10803194
LOC105373262
1 244286121 intergenic variant A/G;T snv 0.35 1