Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10002268 1.000 0.080 4 55653725 intergenic variant T/C snv 0.41 1
rs12542990 1.000 0.080 8 81122216 intergenic variant G/C snv 0.32 1
rs17028375 1.000 0.080 2 64085008 downstream gene variant T/C snv 0.11 1
rs6123557 1.000 0.080 20 56232196 intergenic variant C/T snv 0.21 1
rs7726463 1.000 0.080 5 37954971 intron variant T/C snv 9.1E-02 1
rs11066008
ACAD10
1.000 0.080 12 111702865 intron variant A/G snv 9.1E-03 1
rs17168865
CHRM2 ; LOC349160
1.000 0.080 7 136998465 intron variant T/C snv 5.5E-02 1
rs2231917
FBXO4
1.000 0.080 5 41925333 missense variant C/G snv 2.0E-02 1.1E-02 1
rs2833473
FBXW11P1
1.000 0.080 21 31627241 non coding transcript exon variant G/A snv 0.13 1
rs413812
HSP90AA6P
1.000 0.080 4 170588298 intron variant T/C snv 0.76 1
rs7982141
HSPH1
1.000 0.080 13 31136218 3 prime UTR variant C/A;T snv 1
rs6062927
KCNQ2
1.000 0.080 20 63424660 intron variant G/A snv 0.21 1
rs11265282
LOC105371464 ; FCRL6
1.000 0.080 1 159804618 intron variant T/C snv 0.26 1
rs11184738
LOC105378885
1.000 0.080 1 106056773 intron variant G/A snv 7.3E-02 1
rs8120594
NANP
1.000 0.080 20 25619019 intron variant A/G snv 0.17 1
rs10786161
NOC3L
1.000 0.080 10 94347914 intron variant C/T snv 0.31 1
rs10882430
NOC3L ; PLCE1
1.000 0.080 10 94330915 3 prime UTR variant A/G snv 0.31 1
rs11187876
NOC3L ; PLCE1
1.000 0.080 10 94330382 3 prime UTR variant C/T snv 0.31 1
rs11187844
PLCE1
1.000 0.080 10 94296872 intron variant C/A snv 0.12 1
rs11187853
PLCE1
1.000 0.080 10 94312471 intron variant G/A;C snv 1
rs10882424
PLCE1 ; NOC3L
1.000 0.080 10 94326321 intron variant T/G snv 0.31 1
rs6583937
PLCE1 ; NOC3L
1.000 0.080 10 94323695 intron variant A/G snv 0.32 1
rs917112
PLOD3
1.000 0.080 7 101213710 intron variant T/C snv 1.1E-02 1
rs17090828
SLC22A17
1.000 0.080 14 23350604 intron variant C/G snv 5.1E-02 1
rs11934363
SLC2A9
1.000 0.080 4 9910477 intron variant A/G snv 0.24 1