Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs71297631
TEX9
15 56369974 intron variant -/A ins 2
rs35113840
ILKAP
2 238193015 intron variant -/A;AA delins 2
rs112329286
SYNE2
1.000 0.080 14 63773159 intron variant -/ATTT delins 0.24 4
rs555594022 20 36983292 intergenic variant -/C ins 2
rs34595852 9 86263457 upstream gene variant -/CT delins 0.75 2
rs3840870
COL1A1
17 50184820 3 prime UTR variant -/CTTG delins 13
rs112908525
CD36
7 80675962 intron variant -/GGGTTGAGA delins 0.38 3
rs201184664
TUBD1
17 59873258 intron variant -/GT delins 2
rs150803770 3 49432529 upstream gene variant -/GTTTATTT;TTTTATTT;TTTTATTTATTT;TTTTATTTATTTATTT;TTTTATTTATTTATTTATTT delins 2
rs79237498
RAC1
7 6397234 intron variant -/T;TT delins 2
rs548223088
RBL1
20 37035116 intron variant -/TA ins 2
rs35995659
LINC00216 ; PSMA3-AS1 ; ARMH4
14 58287055 intron variant -/TT ins 0.82 2
rs200980971
CCDC162P
6 109261139 intron variant A/-;AA delins 2
rs2857078
SLC4A1
17 44252803 intron variant A/C snv 0.62 5
rs4953318
PRKCE
2 46127912 intron variant A/C snv 0.43 5
rs11244669
DHX32 ; BCCIP
10 125844213 intron variant A/C snv 0.28 4
rs34338164
PLEK
2 68388414 missense variant A/C snv 8.0E-03 7.8E-03 4
rs138665726
UBE2L3
22 21563570 intron variant A/C snv 0.17 3
rs17302154 2 196183605 intergenic variant A/C snv 9.8E-02 3
rs3169166
DNAJA4
15 78270761 intron variant A/C snv 0.42 3
rs10516140
SQSTM1
5 179813910 intron variant A/C snv 0.76 2
rs10923398 1 117708553 regulatory region variant A/C snv 0.16 2
rs10952780
EZH2
7 148857243 intron variant A/C snv 0.46 2
rs11103379
LHX3
9 136205504 upstream gene variant A/C snv 0.48 2
rs111929233
LOC105370051
12 124893863 intergenic variant A/C snv 9.5E-02 2