Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs201921722 0.925 0.040 11 123679999 downstream gene variant -/A delins 9.2E-06 3
rs34177316
LOC107986273 ; APBB2
0.925 0.040 4 40985283 intron variant A/-;AA;AAA delins 3
rs11039409
NUP160
1.000 0.040 11 47814169 intron variant A/C snv 0.22 2
rs56403421 1.000 0.040 18 55098052 regulatory region variant A/C snv 0.26 2
rs600011
BBX
1.000 0.040 3 107576545 intron variant A/C snv 0.25 2
rs72788286
ATAD2B
1.000 0.040 2 23875451 intron variant A/C snv 0.12 2
rs77607745 1.000 0.040 13 69001052 intergenic variant A/C snv 0.15 2
rs2522833
PCLO
0.827 0.080 7 82824392 missense variant A/C snv 0.45 0.34 1
rs1875560
DCC
1.000 0.040 18 53434318 intron variant A/C;G snv 2
rs9930139
RBFOX1
1.000 0.040 16 7239569 intron variant A/C;T snv 2
rs1344706
ZNF804A
0.701 0.160 2 184913701 intron variant A/C;T snv 1
rs4625
DAG1
0.716 0.280 3 49534707 3 prime UTR variant A/G snv 0.30 17
rs7225002
KANSL1
0.925 0.080 17 46111701 intron variant A/G snv 0.39 7
rs12938031
LINC02210-CRHR1
0.851 0.160 17 45777136 intron variant A/G snv 0.26 4
rs199505
WNT3 ; LRRC37A2
0.925 0.120 17 46782044 intron variant A/G snv 0.84 4
rs7107356 1.000 0.040 11 47654618 downstream gene variant A/G snv 0.45 4
rs143405544
ADAMTS6
0.925 0.040 5 65459777 intron variant A/G snv 4.8E-03 3
rs182377406 0.925 0.040 11 67449378 upstream gene variant A/G snv 4.5E-04 3
rs34467936 1.000 0.040 11 47893747 intergenic variant A/G snv 0.30 3
rs61572747 1.000 0.040 17 45383525 regulatory region variant A/G snv 0.25 3
rs7104036
RAPSN
1.000 0.040 11 47440589 intron variant A/G snv 0.31 3
rs77945277
BAZ1A
0.925 0.040 14 34840969 intron variant A/G snv 4.9E-03 3
rs80164876
LOC105374732 ; EGFLAM
1.000 0.040 5 38464142 3 prime UTR variant A/G snv 1.9E-02 3
rs11039149
NR1H3
0.827 0.280 11 47255124 intron variant A/G snv 0.19 2
rs12068879
KAZN
1.000 0.040 1 14959860 intron variant A/G snv 0.18 2