Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1467568
SIRT1
0.776 0.320 10 67915401 intron variant A/G snv 0.46 8
rs1501899
CASR
0.790 0.240 3 122188481 intron variant A/G snv 0.62 8
rs4293393
UMOD
0.827 0.200 16 20353266 intron variant A/G snv 0.20 8
rs121908525
AGXT
0.790 0.160 2 240875159 missense variant T/C snv 4.4E-05 5.6E-05 7
rs6449213
SLC2A9 ; LOC105374476
0.827 0.240 4 9992591 intron variant C/T snv 0.82 7
rs6553010
LOC105377596 ; MTNR1A
0.851 0.240 4 186535189 intron variant G/A snv 0.23 7
rs737267
SLC2A9
0.851 0.240 4 9933120 intron variant G/A;T snv 7
rs1014290
SLC2A9 ; LOC105374476
0.827 0.280 4 10000237 intron variant G/A snv 0.72 6
rs10509291 0.827 0.280 10 67875446 downstream gene variant T/A snv 7.1E-02 6
rs13140012
LOC105377596 ; MTNR1A
0.827 0.320 4 186544404 intron variant T/A snv 0.41 6
rs1555523841
ABCC6
0.882 0.280 16 16223398 splice donor variant C/A snv 6
rs757343
VDR
0.807 0.360 12 47845892 intron variant C/T snv 0.12 6
rs7955866
FGF23
0.807 0.240 12 4370383 missense variant G/A snv 0.13 0.11 6
rs12654812
RGS14
0.925 0.120 5 177367190 intron variant G/A snv 0.34 5
rs3818292
SIRT1
0.827 0.280 10 67907144 intron variant A/G snv 7.1E-02 5
rs7135617
ORAI1
0.827 0.240 12 121631099 intron variant T/C;G snv 5
rs733175
SLC2A9
0.851 0.240 4 10048517 intron variant C/T snv 0.77 5
rs11746443
RGS14
0.882 0.120 5 177371305 intron variant G/A snv 0.24 0.21 4
rs121964880
VAX2 ; ATP6V1B1
0.851 0.280 2 70958113 missense variant T/C snv 4.0E-06 4
rs12313273
ORAI1
0.882 0.160 12 121625105 upstream gene variant T/C snv 0.23 4
rs151340624
CLCN5
0.851 0.120 X 50090846 stop gained C/T snv 4
rs184187143
SLC26A6
0.882 0.200 3 48628699 missense variant C/A;G snv 1.8E-03 1.6E-03 4
rs4236
C12orf60 ; MGP
0.925 0.120 12 14882147 missense variant T/A;C snv 0.37 4
rs5896
F2
0.882 0.160 11 46723453 missense variant C/G;T snv 0.21 4
rs7456421
HIPK2
0.882 0.120 7 139715976 synonymous variant G/C snv 0.27 0.37 4