Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7107356 1.000 0.040 11 47654618 downstream gene variant A/G snv 0.45 4
rs112538845 0.925 0.040 4 184084475 downstream gene variant C/T snv 1.7E-02 3
rs201921722 0.925 0.040 11 123679999 downstream gene variant -/A delins 9.2E-06 3
rs34102224 0.925 0.040 8 5364506 downstream gene variant G/C snv 0.12 3
rs13296664 1.000 0.040 9 117684418 downstream gene variant C/T snv 0.22 2
rs76923064 1.000 0.040 2 156300636 downstream gene variant T/C snv 1.2E-02 2
rs6774721 1.000 0.040 3 49344465 upstream gene variant G/A snv 0.15 4
rs111365677 0.925 0.040 1 99463578 upstream gene variant T/C snv 2.3E-03 3
rs182377406 0.925 0.040 11 67449378 upstream gene variant A/G snv 4.5E-04 3
rs1994321 1.000 0.040 11 12065766 upstream gene variant G/T snv 0.33 3
rs7613360 1.000 0.040 3 49879277 upstream gene variant C/T snv 0.32 3
rs4578918 1.000 0.040 20 46093017 upstream gene variant T/C snv 0.77 2
rs7713917 0.925 0.040 5 79533426 upstream gene variant A/G snv 0.54 1
rs2298489
TTC12
1.000 0.040 11 113364697 splice region variant A/G snv 0.61 2
rs841
GCH1
0.827 0.200 14 54843774 splice region variant G/A snv 0.22 0.22 1
rs4625
DAG1
0.716 0.280 3 49534707 3 prime UTR variant A/G snv 0.30 17
rs80164876
LOC105374732 ; EGFLAM
1.000 0.040 5 38464142 3 prime UTR variant A/G snv 1.9E-02 3
rs1055447
ARFGAP2 ; C11orf49
1.000 0.040 11 47164873 3 prime UTR variant C/A;T snv 2
rs9586
KLHDC8B
1.000 0.040 3 49176204 3 prime UTR variant C/G;T snv 2
rs35755513
CSNK1G1
1.000 0.040 15 64355987 splice donor variant C/T snv 5.3E-02 2
rs200855945
SSPN ; BHLHE41
0.925 0.040 12 26124961 5 prime UTR variant ACACGCACAC/-;ACACGCACACACACGCACAC delins 1.6E-02 3
rs10405382
DPY19L3 ; LOC400684
1.000 0.040 19 32405810 5 prime UTR variant C/G snv 0.18 2
rs2251219
SMIM4 ; PBRM1
0.732 0.120 3 52550771 synonymous variant T/C;G snv 0.39; 4.0E-06 0.34 3
rs754593
MAPT
1.000 0.040 17 45977330 non coding transcript exon variant G/A snv 0.52 4
rs13381817
TCF4
1.000 0.040 18 55230988 non coding transcript exon variant C/T snv 6.2E-02 2