Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs79246196
STAG3
0.925 0.080 7 100185286 intron variant C/T snv 1.8E-02 4
rs57083693
UTP20
1.000 0.080 12 101348402 intron variant T/C snv 0.23 3
rs12544026
NCALD
0.925 0.080 8 101819970 intron variant G/A snv 0.85 4
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 30
rs115357105 0.925 0.080 9 104376689 intergenic variant A/G snv 1.5E-02 4
rs61776290 1.000 0.080 1 10634850 upstream gene variant C/T snv 8.7E-02 3
rs7906104
LINC02661
1.000 0.080 10 108737343 intron variant C/T snv 0.29 3
rs1995364 1.000 0.080 5 10903669 intergenic variant A/G snv 0.62 1
rs17125651 1.000 0.080 10 109063325 intergenic variant T/C snv 0.14 3
rs3782886
BRAP
0.724 0.480 12 111672685 synonymous variant T/C snv 1.9E-02 5.9E-03 11
rs11066001
BRAP
0.763 0.360 12 111681367 intron variant T/C snv 5.8E-03 5
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 29
rs143894582
PTPN11
1.000 0.080 12 112469070 intron variant A/-;AA delins 1
rs61902812 1.000 0.080 11 113503698 intergenic variant C/A snv 0.26 3
rs4936277 1.000 0.080 11 113561238 intergenic variant A/G snv 0.37 3
rs141424017 1.000 0.080 7 115311376 intergenic variant -/CAA ins 3
rs7777391 1.000 0.080 7 117981823 intergenic variant A/G snv 0.60 1
rs6777876 1.000 0.080 3 11915124 upstream gene variant A/G snv 9.9E-02 3
rs1316543
GRK5
1.000 0.080 10 119445148 intron variant G/A snv 0.15 3
rs2002594
FAM162A
1.000 0.080 3 122392714 intron variant A/G snv 0.59 3
rs34997829
LHPP
1.000 0.080 10 124546821 intron variant G/C snv 0.24 3
rs750338
PKNOX2
1.000 0.080 11 125302697 intron variant A/G snv 0.30 3
rs17616845 1.000 0.080 7 12741918 intron variant T/C snv 0.15 1
rs72716801 1.000 0.080 8 127636481 non coding transcript exon variant G/T snv 5.5E-02 3
rs1660895 1.000 0.080 2 129236759 intergenic variant A/T snv 0.52 3