Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7158768
FBXO34
14 55296894 intron variant A/C;T snv 1
rs8016239
LOC107984664 ; TBPL2
14 55427866 intron variant A/C;T snv 1
rs687289
ABO
1.000 0.120 9 133261703 intron variant A/G snv 15
rs2657879
GLS2 ; SPRYD4
1.000 0.080 12 56471554 missense variant A/G snv 0.17 0.15 9
rs2169387
LOC157273
8 9323885 intron variant A/G snv 0.87 6
rs17128183 0.882 0.120 14 55112795 intergenic variant A/G snv 0.57 5
rs4273077
TNFRSF13B
0.925 0.160 17 16945825 intron variant A/G snv 0.13 4
rs641943
ABO
9 133258323 intron variant A/G snv 0.29 4
rs8176732
ABO
9 133256916 intron variant A/G snv 0.25 3
rs1718309
PAH
12 102848618 intron variant A/G snv 0.67 2
rs28645201
CCSER1
4 90607776 intron variant A/G snv 3.7E-02 2
rs34226052 4 88242371 intergenic variant A/G snv 0.22 2
rs4470077
LOC107984664 ; TBPL2
14 55430820 intron variant A/G snv 0.29 2
rs4554975
SLC38A4
12 46808031 intron variant A/G snv 0.47 2
rs10133662
GCH1
14 54849552 intron variant A/G snv 0.45 1
rs10135789 14 54825302 intergenic variant A/G snv 0.45 1
rs10140164
WDHD1
14 54939405 3 prime UTR variant A/G snv 0.50 1
rs10144326
DLGAP5
14 55177190 synonymous variant A/G snv 0.16 0.29 1
rs10150760
FBXO34
14 55354830 intron variant A/G snv 0.42 1
rs11625204 14 55088199 intergenic variant A/G snv 0.26 1
rs11851178
SOCS4
14 55035411 intron variant A/G snv 0.44 1
rs1187874
SOCS4
14 55031385 intron variant A/G snv 0.74 1
rs1188076
KTN1-AS1
14 55507757 intron variant A/G snv 0.35 1
rs17671923 14 55197200 intron variant A/G snv 5.8E-02 1
rs17673930
FBXO34
14 55341433 intron variant A/G snv 5.8E-02 1