Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs59758982
TP53
0.925 0.040 17 7676326 intron variant TCCAGGTCCCCAGCCCTCCAGGTCCCCAGCCC/-;TCCAGGTCCCCAGCCC;TCCAGGTCCCCAGCCCTCCAGGTCCCCAGCCCTCCAGGTCCCCAGCCC delins 0.82 2
rs1801131
MTHFR
0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 93
rs2149356
TLR4
0.742 0.360 9 117711921 intron variant T/G snv 0.54 14
rs504022 1.000 0.040 21 43311258 regulatory region variant T/G snv 0.91 1
rs73174345
MECOM
1.000 0.040 3 169535095 intron variant T/G snv 7.9E-02 1
rs9309969
CADM2
1.000 0.040 3 85085406 intron variant T/C;G snv 2
rs1020338837
AZI2
1.000 0.040 3 28340470 missense variant T/C;G snv 4.0E-06 1
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs564398
CDKN2B-AS1
0.716 0.360 9 22029548 3 prime UTR variant T/C snv 0.31 0.28 18
rs2165241
LOXL1-AS1 ; LOXL1
0.716 0.360 15 73929861 intron variant T/C snv 0.60 15
rs11024102
PLEKHA7
0.851 0.040 11 16987058 intron variant T/C snv 0.20 7
rs3918249
MMP9
0.807 0.200 20 46009497 intron variant T/C snv 0.41 6
rs10483727 0.851 0.040 14 60606157 upstream gene variant T/C snv 0.45 4
rs74315336
MYOCOS ; MYOC
0.851 0.040 1 171636173 missense variant T/C snv 4
rs7859156
LMX1B
0.851 0.040 9 126637749 intron variant T/C snv 0.74 4
rs6475604
CDKN2B-AS1
0.925 0.040 9 22052735 intron variant T/C snv 0.72 3
rs735860
GCM1
0.882 0.040 6 53258320 regulatory region variant T/C snv 0.66 3
rs10281637 1.000 0.040 7 116511284 downstream gene variant T/C snv 0.28 2
rs10918274
TMCO1
1.000 0.040 1 165745179 intron variant T/C snv 0.89 2
rs4141671
BICC1
1.000 0.040 10 58578993 intron variant T/C snv 0.49 2
rs8006686
MTHFD1
0.925 0.040 14 64401953 intron variant T/C snv 0.22 2
rs369115487
CYP1B1-AS1 ; CYP1B1
1.000 0.040 2 38075373 missense variant T/C snv 1.6E-05 1.4E-05 1
rs555091
IMMP1L ; ELP4
1.000 0.040 11 31511412 3 prime UTR variant T/C snv 5.6E-03 1
rs566095092
AZI2
1.000 0.040 3 28336841 missense variant T/C snv 4.0E-06 2.1E-05 1
rs869833
TMEM182
1.000 0.040 2 102766672 intron variant T/C snv 0.49 1