Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs141216986
LOC107985698
X 128594571 intron variant C/T snv 1.7E-02 1
rs4823006
ZNRF3
22 29055683 3 prime UTR variant A/G snv 0.41 5
rs5762862
ZNRF3
22 28856744 intergenic variant G/A;T snv 4
rs4396807
TRIOBP
22 37742372 intron variant G/C snv 0.38 3
rs117222687
COMT ; ARVCF
22 19968491 intron variant G/C snv 3.8E-02 4.1E-02 2
rs12321
ZNRF3
1.000 0.040 22 29057205 3 prime UTR variant G/C snv 0.38 2
rs133980 22 27626764 intergenic variant A/G snv 0.42 2
rs34887403
HSCB
22 28755162 intron variant G/A snv 0.11 2
rs758374
ARVCF
22 19984029 intron variant T/C snv 0.27 2
rs1034565
ARVCF
22 19996688 intron variant C/A;G;T snv 1
rs134186
TTC28
22 28242523 intron variant C/G snv 0.32 1
rs138834
BRD1
22 49786849 intron variant A/C snv 0.22 1
rs139919
TNRC6B
22 40330179 3 prime UTR variant T/C snv 0.20 1
rs2012714
ARVCF
22 19990124 intron variant C/T snv 0.34 1
rs2238787
ARVCF
22 19988883 intron variant G/A snv 0.25 1
rs28578714
PLXNB2
22 50289492 intron variant T/C snv 0.35 0.41 1
rs5992134
MICAL3
22 17951228 intron variant G/T snv 0.26 1
rs73169175
TCF20
22 42325368 intron variant T/G snv 8.2E-02 1
rs9608690
LOC101929594 ; TTC28
22 28525359 intron variant G/A snv 5.6E-02 1
rs2823139 1.000 0.080 21 15204463 intron variant G/A snv 0.34 5
rs9306160
RRP1B
0.925 0.080 21 43687681 missense variant T/C snv 0.69 0.73 5
rs2229742
NRIP1
21 14966851 missense variant G/C snv 7.9E-02 7.1E-02 3
rs112204826 21 43301147 TF binding site variant C/T snv 2.9E-02 2
rs12627651 21 43340723 intergenic variant G/A snv 0.22 2
rs2410182 21 39808149 intergenic variant A/G;T snv 2