Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13175330
PAM
5 102840757 intron variant A/G snv 7.8E-02 2
rs223361
UBE2D3
4 102848147 intron variant T/C snv 0.37 1
rs4409766
BORCS7-ASMT ; BORCS7
1.000 0.040 10 102856906 intron variant T/C snv 0.14 6
rs2513877
AZIN1-AS1 ; AZIN1
8 102871402 intron variant G/A snv 0.25 1
rs17135875
FBXL13
7 102878584 intron variant T/C snv 0.24 3
rs943037
CNNM2
10 103076162 synonymous variant C/T snv 0.12 8.3E-02 2
rs11191548
CNNM2
0.882 0.080 10 103086421 3 prime UTR variant T/C snv 8.6E-02 10
rs7129220
AMPD3 ; CAND1.11
11 10328991 intron variant G/A snv 0.10 5
rs1450271
AMPD3 ; CAND1.11
11 10334568 intron variant C/T snv 0.43 2
rs13390641 2 103419975 intergenic variant G/A snv 0.12 3
rs4387287
STN1
10 103918139 5 prime UTR variant A/C snv 0.69 4
rs111447985
STN1
10 103918153 5 prime UTR variant C/A;T snv 1.1E-02 1
rs11191871
LOC102724351
10 103947673 intergenic variant A/G snv 5.2E-02 2
rs34161718
KIF26A
14 104153856 intron variant C/G;T snv 1
rs3063286
SLX4IP
20 10507905 intron variant TA/-;TATA;TATATA;TATATATA;TATATATATA delins 1
rs191784289
SORCS3
10 105135184 intron variant C/T snv 8.4E-03 2
rs72613227
LOC105377923
6 105872896 intron variant A/T snv 0.10 1
rs35287509
PTPRD
9 10594635 intron variant T/C snv 0.26 1
rs13112725
NPNT
4 105990585 intron variant G/C snv 0.70 2
rs1330225 1 106293321 intergenic variant T/C snv 0.38 3
rs2392929 7 106773623 upstream gene variant T/A;C;G snv 4
rs7020564
ZNF462
9 106907735 intron variant A/C;T snv 1
rs568998724
LOC340512
9 107040156 intron variant G/A snv 6.8E-04 1
rs7951348 11 107211115 intergenic variant C/T snv 0.39 2
rs6995692
SOX7 ; PINX1 ; LOC102723313
8 10729498 non coding transcript exon variant G/C;T snv 0.60 2