Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7632505
SEMA5B
0.827 0.120 3 123019460 intron variant A/G snv 0.34 17
rs113235453
NUBPL
1.000 0.040 14 31849939 intron variant A/G snv 3.5E-02 3
rs139130723 1.000 0.040 6 14411553 intergenic variant A/G snv 4.4E-03 3
rs28763958
DSP
0.882 0.080 6 7558186 missense variant A/G snv 6.4E-05 2.8E-05 3
rs1805126
SCN5A
0.925 0.040 3 38550915 synonymous variant A/G snv 0.39 0.44 2
rs3212247
RIPK3
0.925 0.040 14 24340589 upstream gene variant A/G snv 0.12 2
rs6787362
FRMD4B
0.925 0.040 3 69178228 intron variant A/G snv 9.3E-02 2
rs11172782 1.000 0.040 12 58865846 intergenic variant A/G snv 0.12 1
rs1136201
ERBB2
0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 34
rs1800624
PBX2 ; AGER
0.658 0.480 6 32184610 upstream gene variant A/G;T snv 33
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv 22
rs1728918 0.827 0.160 2 27412596 upstream gene variant A/G;T snv 19
rs7115242
SIK3
0.851 0.120 11 117037567 intron variant A/G;T snv 16
rs1799998
CYP11B2
0.742 0.200 8 142918184 upstream gene variant A/G;T snv 0.38 14
rs5068
NPPA ; NPPA-AS1 ; CLCN6
0.776 0.160 1 11845917 3 prime UTR variant A/G;T snv 13
rs460976 0.851 0.120 21 41463567 downstream gene variant A/G;T snv 7
rs57045855
LMNA
0.882 0.040 1 156134464 missense variant A/G;T snv 6
rs267607499
DES
0.851 0.160 2 219418809 missense variant A/G;T snv 4
rs12638540
CMTM7
1.000 0.040 3 32447042 intron variant A/G;T snv 1
rs1800730
HFE ; LOC108783645
0.649 0.480 6 26090957 missense variant A/T snv 1.0E-02 1.0E-02 32
rs2866611 0.851 0.120 20 41322165 upstream gene variant A/T snv 0.58 16
rs2230345
GRK5
0.807 0.160 10 119326585 missense variant A/T snv 3.8E-02 9.0E-02 6
rs1028728
POSTN
0.925 0.040 13 37599679 upstream gene variant A/T snv 0.20 3
rs1700575
LOC105374647
1.000 0.040 5 8543925 intron variant A/T snv 0.26 3
rs2210327
ADAMTSL1
1.000 0.040 9 18109237 intron variant A/T snv 3.4E-02 1