Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6851943
LOC101929353
4 100203265 intron variant G/T snv 0.44 2
rs241812
SIM1 ; LOC102724406
6 100443115 intron variant A/G;T snv 2
rs1044261
GTPBP4 ; IDI2
1.000 0.080 10 1019770 stop gained C/T snv 5.0E-02 6.0E-02 3
rs75174967
SUFU
10 102517336 intron variant G/A snv 8.2E-03 2
rs151134704
NFKB1 ; LOC105377347
4 102616435 splice region variant C/T snv 1.6E-04 9.1E-05 3
rs228611
MANBA
4 102640552 intron variant G/A snv 0.40 2
rs56121637
RNF128
X 106773038 missense variant A/T snv 5.8E-03 5.2E-03 2
rs10127790
SORT1
1 109348511 intron variant C/T snv 0.63 2
rs1933182 1.000 0.080 1 109457216 intergenic variant A/C snv 0.63 3
rs12136063
SYPL2
1 109471548 intron variant G/A snv 0.60 2
rs7971845
TRPV4
12 109822897 intron variant C/G snv 0.35 1
rs10794720
WDR37
1.000 0.080 10 1110225 intron variant T/C snv 0.89 4
rs79105258
CUX2
12 111280427 intron variant C/A;T snv 24
rs12144044
RHOC
1 112706169 5 prime UTR variant C/A;G snv 0.24 2
rs11123169
PSD4
1.000 0.080 2 113209498 upstream gene variant C/A;T snv 3
rs13298297
ASTN2
9 116501829 intron variant G/A snv 0.21 2
rs307558
SYN2
3 12053630 intron variant G/A snv 0.75 2
rs17050272
LOC105373585
0.882 0.120 2 120548864 upstream gene variant G/A snv 0.33 9
rs2789047 6 120868656 intergenic variant C/A;G;T snv 1
rs36096257
TFCP2L1
2 121281207 missense variant G/A snv 6.8E-03 2.9E-03 3
rs10277115 7 1245559 regulatory region variant A/T snv 0.57 2
rs62435145 1.000 0.040 7 1246931 regulatory region variant G/T snv 0.51 8
rs1533988 7 1253374 intergenic variant A/T snv 0.59 6
rs75834729
CCDC26
8 129359392 intron variant C/G;T snv 2
rs2781656
ARG1
6 131561431 intron variant C/T snv 0.39 2