Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1739843
HSPB7
0.882 0.040 1 16016759 intron variant T/C snv 0.62 4
rs198358
NPPA-AS1 ; CLCN6
0.925 0.040 1 11844019 3 prime UTR variant T/C snv 0.32 4
rs2549513
MAF
0.851 0.080 16 79516830 downstream gene variant C/A;T snv 4
rs267607499
DES
0.851 0.160 2 219418809 missense variant A/G;T snv 4
rs499818 0.851 0.080 6 13332235 upstream gene variant G/A snv 0.21 4
rs587782927
DSP
0.882 0.080 6 7574084 splice region variant AG/- delins 4
rs61661343
LMNA
0.851 0.040 1 156130687 missense variant T/C snv 4
rs9351814 0.882 0.040 6 71484004 intergenic variant A/C snv 0.35 4
rs9838915
KLF15
0.882 0.120 3 126347377 intron variant G/A snv 0.19 4
rs1028728
POSTN
0.925 0.040 13 37599679 upstream gene variant A/T snv 0.20 3
rs10501920
CNTN5
0.882 0.080 11 99622442 intron variant C/G snv 0.14 3
rs1249958
PPP1R1A
0.925 0.040 12 54582053 missense variant C/T snv 2.7E-02 3
rs1253810269
ARID1A
0.882 0.080 1 26696971 missense variant G/A snv 7.0E-06 3
rs1258130495
EDNRA
0.882 0.040 4 147485727 missense variant G/A snv 3
rs1303946678
CYP2D6 ; NDUFA6-DT
0.925 0.040 22 42126851 missense variant C/G snv 3
rs243864
MMP2
0.925 0.080 16 55478410 intron variant T/G snv 0.19 3
rs6026584
GNAS
0.925 0.040 20 58894018 intron variant T/C snv 0.70 3
rs794728602
LMNA
1.000 0.040 1 156115168 missense variant G/A snv 3
rs899115126
EDNRA
0.882 0.080 4 147542603 missense variant G/C snv 3
rs958546
LRRC63
0.882 0.040 13 46259582 intron variant G/C snv 0.29 3
rs10932374
ERBB4
0.925 0.040 2 211379678 3 prime UTR variant G/A snv 0.23 2
rs13003941
ERBB4
0.925 0.040 2 211378978 3 prime UTR variant G/C;T snv 0.26 2
rs1337916669
LOC108783645 ; HFE
0.925 0.040 6 26092879 missense variant G/T snv 2
rs1595064
ERBB4
0.925 0.040 2 211378020 3 prime UTR variant G/A;C snv 2
rs1595065
ERBB4
0.925 0.040 2 211377916 3 prime UTR variant G/A snv 0.73 2