Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2228001
XPC
0.570 0.480 3 14145949 missense variant G/T snv 0.63 0.65 60
rs7651446
TIPARP
0.882 0.120 3 156689208 intron variant G/T snv 7.9E-02 3
rs1192691 0.925 0.120 10 36880367 regulatory region variant G/T snv 0.90 2
rs7643459
LOC101927394 ; LMCD1-AS1
0.925 0.120 3 7963141 intron variant G/C;T snv 2
rs74917072
UBE2F ; UBE2F-SCLY
0.882 0.120 2 238022053 intron variant G/A;T snv 3
rs1413299
COL15A1
0.925 0.120 9 98998959 intron variant G/A;T snv 2
rs41324349
CARD11
0.925 0.120 7 2907529 intron variant G/A;C;T snv 2
rs104886003
PIK3CA
0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 71
rs7405776
HNF1B
0.807 0.120 17 37733029 intron variant G/A;C snv 6
rs1649942
NRG3
0.925 0.120 10 82191935 intron variant G/A;C snv 3
rs3745546
INSR
0.925 0.120 19 7211805 intron variant G/A;C snv 2
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1222213359
VEGFA
0.574 0.720 6 43770966 missense variant G/A snv 62
rs4759314
HOTAIR
0.649 0.440 12 53968051 non coding transcript exon variant G/A snv 0.93 31
rs8170
BABAM1 ; USHBP1
0.724 0.160 19 17278895 synonymous variant G/A snv 0.15 0.18 13
rs10088218
LINC00824
0.851 0.120 8 128531703 intron variant G/A snv 0.13 4
rs183211
LRRC37A2 ; NSF
0.882 0.160 17 46710944 intron variant G/A snv 0.28 0.30 4
rs1002076
KIF1B
0.925 0.120 1 10378834 3 prime UTR variant G/A snv 0.33 2
rs1017134 0.925 0.120 7 35307237 intergenic variant G/A snv 0.47 2
rs11175194
SRGAP1
0.925 0.120 12 63871057 intron variant G/A snv 0.15 2
rs17250239
TRAF2
0.925 0.120 9 136902178 non coding transcript exon variant G/A snv 7.2E-02 2
rs2803073
PRKN
0.925 0.120 6 162541796 intron variant G/A snv 0.74 2
rs3087714
SULF1
0.925 0.120 8 69660769 3 prime UTR variant G/A snv 0.30 2
rs7305032
VDR
0.925 0.120 12 47856077 intron variant G/A snv 0.61 2
rs12039431
RSPO1
1.000 0.120 1 37616450 intron variant G/A snv 0.24 0.21 1