Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1536895 1.000 0.080 9 104031445 intergenic variant A/G snv 9.5E-02 1
rs121909574
TFAP2A-AS2 ; TFAP2A
0.724 0.400 6 10404509 missense variant T/A;C;G snv 4.6E-06 17
rs793888541
TFAP2A-AS2 ; TFAP2A
0.807 0.120 6 10404631 missense variant A/T snv 7
rs9653456
RANBP2
1.000 0.080 2 109029903 intergenic variant A/C;G snv 1
rs12229654 0.763 0.320 12 110976657 intergenic variant T/G snv 4.8E-03 20
rs11066150
NAA25
0.925 0.120 12 112080999 intron variant G/A snv 1.3E-02 2
rs12229892
PTPN11
0.807 0.240 12 112485589 intron variant G/A snv 1.4E-02 6
rs7078160
SHTN1
0.851 0.120 10 117068049 intron variant G/A snv 0.19 4
rs4752028
SHTN1
0.807 0.200 10 117075480 intron variant C/T snv 0.73 6
rs10886040
SHTN1
0.882 0.120 10 117086783 intron variant C/G snv 0.20 3
rs6585429
VAX1
0.925 0.120 10 117133720 3 prime UTR variant A/G snv 0.68 2
rs2294426
ADTRP
1.000 0.080 6 11729849 intron variant A/G;T snv 1
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs7554547 0.925 0.120 1 11913831 non coding transcript exon variant A/G;T snv 2
rs1269636220
WDR11
0.851 0.280 10 120865109 missense variant A/G snv 5
rs1057518960
GJA1
0.882 0.160 6 121447333 missense variant G/C snv 7
rs7692299
LINC01091
0.925 0.120 4 123789429 intron variant C/T snv 0.15 2
rs908822 0.925 0.120 4 123985102 regulatory region variant C/A;T snv 2
rs1372995 1.000 0.080 8 128630121 downstream gene variant T/C snv 4.1E-02 1
rs7015145
CCDC26
1.000 0.080 8 128697039 intron variant A/G snv 0.67 1
rs1432017
CCDC26
1.000 0.080 8 128723840 intron variant C/T snv 0.32 1
rs9297775
CCDC26
1.000 0.080 8 128724466 intron variant C/A snv 0.32 1
rs1030608
CCDC26
1.000 0.080 8 128727506 intron variant G/A snv 0.47 1
rs1030609
CCDC26
1.000 0.080 8 128727631 intron variant C/A;G snv 1