Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs143558304
TPM4
19 16102887 3 prime UTR variant -/A delins 4.6E-02 2
rs75140056 6 29640407 upstream gene variant -/A;AT ins 0.60 1
rs11471957
TUBB1
20 59023277 intron variant -/AA ins 2
rs111350029
PIEZO1 ; LOC100289580
16 88730362 intron variant -/AGGCGG delins 1
rs3840870
COL1A1
17 50184820 3 prime UTR variant -/CTTG delins 13
rs11446839 9 38198231 intergenic variant -/G delins 0.48 1
rs10661645
NAA25
12 112086916 intron variant -/GAG;GGAG delins 0.95 1
rs10654220
MPHOSPH9
1.000 0.040 12 123218875 intron variant -/TGT;TGTTGT delins 2
rs56318916
DOCK8
9 329344 intron variant A/- del 0.22 2
rs11294619
PAK2
3 196784238 intron variant A/- delins 1
rs11405616
NDFIP1
5 142130697 intron variant A/-;AA;AAA;AAAA delins 4
rs10820606 9 96430637 intergenic variant A/C snv 0.23 2
rs1331308
HBS1L
6 135083984 intron variant A/C snv 0.61 2
rs80012730 12 49277876 upstream gene variant A/C snv 6.1E-02 2
rs112790992
BRF1
14 105291880 intron variant A/C snv 0.31 1
rs2365726
PTPRH
19 55186797 intron variant A/C snv 0.43 1
rs36109901
CBL
11 119212608 intron variant A/C snv 0.27 1
rs4731120
HYAL4
7 123771169 intergenic variant A/C snv 6.5E-02 1
rs7146395
YLPM1
14 74761944 upstream gene variant A/C snv 0.68 1
rs75080135
GGNBP1
6 33584930 intron variant A/C snv 0.17 1
rs7856073 9 4891797 intergenic variant A/C snv 0.49 1
rs9974653
LOC105372804
21 39369920 downstream gene variant A/C snv 0.34 1
rs112505971
ANKRD26
10 27068541 intron variant A/C;G snv 13
rs1801689
APOH
17 66214462 missense variant A/C;G snv 4.0E-06; 2.4E-02; 4.8E-05 7
rs141759085
RAB11FIP3
16 480967 intron variant A/C;G snv 0.25 1