Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs55705857
CCDC26
0.732 0.080 8 129633446 intron variant A/G snv 3.9E-02 4
rs6020712
CTNNBL1
1.000 0.080 20 37758210 intron variant G/A snv 0.12 4
rs6763931
ZBTB38
0.925 0.080 3 141383991 intron variant G/A snv 0.54 4
rs16986921
CTNNBL1
1.000 0.080 20 37754119 intron variant C/T snv 0.12 3
rs17632542
KLK3
0.925 0.080 19 50858501 missense variant T/C snv 5.5E-02 4.9E-02 3
rs80359540
BRCA2
0.925 0.080 13 32340176 frameshift variant A/- delins 3
rs8176704
ABO
0.925 0.080 9 133260148 intron variant G/A snv 3
rs10187424
VAMP8
0.925 0.080 2 85567174 intron variant T/A;C snv 2
rs10503733
LOC107986930
0.925 0.080 8 23676505 downstream gene variant G/T snv 0.27 2
rs10505483
PCAT1 ; CASC19
0.925 0.080 8 127112950 intron variant C/T snv 0.16 2
rs1058205
KLK3
0.925 0.080 19 50860142 3 prime UTR variant C/T snv 0.75 0.74 2
rs10875943 0.925 0.080 12 49282227 intergenic variant T/A;C snv 2
rs10936632 0.925 0.080 3 170412314 intron variant C/A snv 0.41 2
rs11102001
GSTM5 ; EPS8L3
0.925 0.080 1 109757069 missense variant G/A snv 9.4E-02 0.16 2
rs11135910
EBF2
0.925 0.080 8 26034626 intron variant C/T snv 0.13 2
rs11199874 0.925 0.080 10 121273005 intergenic variant G/A snv 0.23 2
rs11650494 0.925 0.080 17 49267824 intron variant G/A snv 0.12 2
rs11672691
PCAT19
0.925 0.080 19 41479679 non coding transcript exon variant G/A snv 0.42 2
rs11704416
FAM83F
0.925 0.080 22 40040969 3 prime UTR variant G/C snv 0.21 2
rs11902236
GRHL1
0.925 0.080 2 9977740 intron variant C/T snv 0.36 2
rs119484086
ELAC2
0.851 0.080 17 12992957 missense variant C/A;T snv 4.0E-06; 5.3E-04 2
rs12155172
LINC01162
0.925 0.080 7 20954872 intron variant A/G snv 0.81 2
rs1218582
KCNN3
0.925 0.080 1 154861707 intron variant G/A snv 0.46 2
rs12653946
CTD-2194D22.4
0.882 0.080 5 1895715 intron variant C/T snv 0.43 2
rs1270884 0.925 0.080 12 114247766 intergenic variant A/G snv 0.63 2