Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800802
MGP ; C12orf60
0.925 0.040 12 14885985 intron variant A/G snv 0.15 3
rs1871054
ADAM12
0.925 0.040 10 126093840 intron variant C/A;T snv 3
rs2289263
SMAD3
0.925 0.120 15 67146869 intron variant T/G snv 0.43 3
rs2615977
COL11A1
0.925 0.080 1 102986836 intron variant A/C snv 0.27 3
rs2622873
COL11A1
0.882 0.040 1 103000497 intron variant T/C;G snv 3
rs3830675
PTEN
1.000 0.040 10 87931195 intron variant -/TCTTA delins 3
rs715572
TIMP3 ; SYN3
0.925 0.040 22 32838944 intron variant G/A snv 0.18 3
rs75621460
TGFB1
0.882 0.040 19 41327879 intron variant G/A snv 2.0E-02 3
rs10654220
MPHOSPH9
1.000 0.040 12 123218875 intron variant -/TGT;TGTTGT delins 2
rs115740542
H2AC6 ; H2BC4
0.925 0.040 6 26123274 intron variant T/C snv 3.6E-02 2
rs13301537
ASPN ; CENPP
0.925 0.040 9 92466765 intron variant A/G snv 0.38 2
rs1905786
TNFRSF11B
1.000 0.040 8 118939453 intron variant T/A;C snv 2
rs3771501
TGFA
0.925 0.040 2 70490521 intron variant A/G snv 0.60 2
rs4238326
ALDH1A2
0.925 0.040 15 58043802 intron variant T/C snv 0.28 2
rs4907986
COL11A1
0.925 0.040 1 103084077 intron variant C/T snv 0.49 2
rs6494629
SMAD3
0.925 0.120 15 67081773 intron variant C/T snv 0.52 2
rs7164503
ANP32A
0.925 0.040 15 68789051 intron variant T/C snv 0.27 2
rs835487
CHST11
0.925 0.040 12 104666989 intron variant A/G snv 0.43 2
rs912428
LRCH1
0.925 0.040 13 46593768 intron variant A/G snv 0.84 2
rs10172410
ITGA4
1.000 0.040 2 181487841 intron variant T/C snv 0.45 1
rs10218792
KIF26B
1.000 0.040 1 245587630 intron variant T/G snv 0.26 1
rs1032128
TNFRSF11B
1.000 0.040 8 118939534 intron variant G/A snv 0.30 1
rs1034762
COL2A1
1.000 0.040 12 47995860 intron variant A/C snv 0.74 0.79 1
rs10401670
MCEMP1
1.000 0.040 19 7677916 intron variant T/C;G snv 0.49 1
rs10502437
TMEM241
1.000 0.040 18 23390742 intron variant G/A snv 0.30 1