Source: CURATED

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11067228 0.925 0.080 12 114656455 downstream gene variant A/G snv 0.37 1
rs114918764 1.000 0.080 4 116449550 intergenic variant C/T snv 2.0E-03 1
rs1543175
LSAMP
1.000 0.080 3 116668062 intron variant G/A snv 0.45 1
rs13325108
LSAMP
1.000 0.080 3 116671823 intron variant C/A;G snv 1
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 38
rs339331
RFX6
0.882 0.080 6 116888889 intron variant T/C snv 0.28 2
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 6
rs1801131
MTHFR
0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 1
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 6
rs9651118
MTHFR
0.683 0.480 1 11802157 intron variant T/C snv 0.18 2
rs12537079 1.000 0.080 7 118064652 intergenic variant T/A;G snv 1
rs11199874 0.925 0.080 10 121273005 intergenic variant G/A snv 0.23 2
rs1801725
CASR
0.633 0.600 3 122284910 missense variant G/T snv 0.13 0.11 2
rs1042636
CASR
0.672 0.360 3 122284922 missense variant A/G snv 0.15 9.0E-02 1
rs13083990 0.925 0.080 3 122295719 downstream gene variant T/C snv 0.30 2
rs13119723
KIAA1109
0.807 0.280 4 122297158 intron variant A/G snv 0.10 5
rs2069762
IL2
0.672 0.560 4 122456825 upstream gene variant A/C snv 0.24 2
rs6822844 0.689 0.520 4 122588266 regulatory region variant G/T snv 0.10 5
rs6840978
IL21-AS1
0.776 0.160 4 122633552 intron variant C/T snv 0.16 6
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 5
rs1805192
PPARG
0.510 0.840 3 12379739 missense variant C/G snv 4
rs4962416
CTBP2
0.882 0.160 10 125008303 intron variant T/C snv 0.23 3
rs62477096
LOC101928283
1.000 0.080 7 125296388 intron variant A/G snv 0.19 1
rs6965492
LOC101928283
1.000 0.080 7 125304928 intron variant G/T snv 0.19 1
rs12543663
LOC105375751 ; PCAT1
1.000 0.080 8 126912414 intron variant C/A;T snv 1