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
rs17792983 1.000 0.040 6 100363657 regulatory region variant C/T snv 0.24 1
rs13122395
EMCN
1.000 0.040 4 100829496 intron variant G/A snv 0.34 2
rs7758630
LOC107984041
1.000 0.040 6 100939428 intergenic variant T/A;C snv 1
rs1722229 1.000 0.040 7 101642897 intergenic variant G/C;T snv 2
rs12544026
NCALD
0.925 0.080 8 101819970 intron variant G/A snv 0.85 4
rs6878284
SLCO6A1
0.925 0.040 5 102434022 intron variant C/T snv 0.64 1
rs11191454
LOC107984265 ; BORCS7-ASMT ; AS3MT
0.776 0.160 10 102900247 intron variant A/G snv 7.9E-02 5
rs7914558
CNNM2
0.851 0.040 10 103016151 intron variant G/A snv 0.40 5
rs117911063
CDC42BPB
1.000 0.040 14 103037856 intron variant C/A;T snv 2.1E-02 1
rs11990063
MSRA
0.925 0.040 8 10307685 intron variant C/A;T snv 3
rs1304150 1.000 0.040 3 103112741 regulatory region variant C/A;G;T snv 1
rs11191580
NT5C2
0.827 0.040 10 103146454 intron variant T/C snv 7.9E-02 12
rs1961982
C12orf42
0.925 0.040 12 103218955 intergenic variant G/A snv 0.27 2
rs188843168
ATP5MD
0.925 0.040 10 103390184 intron variant T/A;C snv 4.3E-04 3
rs10149470 1.000 0.040 14 103551616 upstream gene variant A/G snv 0.54 3
rs4906335 0.925 0.040 14 103554804 intron variant C/A;G snv 2
rs4906349
KLC1
1.000 0.040 14 103624778 intron variant A/G snv 0.36 1
rs6484218
CAND1.11 ; AMPD3
0.882 0.040 11 10369034 intron variant G/A snv 0.21 4
rs2945451 1.000 0.040 2 103852954 downstream gene variant A/T snv 0.30 1
rs77724872 1.000 0.040 12 104360722 intergenic variant C/T snv 4.5E-02 2
rs115357105 0.925 0.080 9 104376689 intergenic variant A/G snv 1.5E-02 4
rs2028526 1.000 0.040 5 104430453 intron variant T/C snv 0.31 1
rs142383097
DFFA
1.000 0.040 1 10461101 3 prime UTR variant A/C;G snv 2.0E-02 2
rs30266
LOC105379109
1.000 0.040 5 104636656 intron variant G/A snv 0.24 1