Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 38
rs121909231
PTEN
0.667 0.600 10 87961095 stop gained C/A;T snv 29
rs7679673 0.677 0.440 4 105140377 intron variant C/A snv 0.50 25
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 25
rs121913286
PIK3CA
0.677 0.280 3 179218306 missense variant C/A;G snv 22
rs10069690
TERT
0.595 0.560 5 1279675 intron variant C/T snv 0.36 19
rs505922
ABO
0.689 0.520 9 133273813 intron variant C/T snv 19
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 19
rs7931342 0.689 0.360 11 69227030 intergenic variant T/G snv 0.58 19
rs121913293
PTEN
0.732 0.360 10 87952142 missense variant C/A;T snv 18
rs2736100
TERT
0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 16
rs863224909
PTEN
0.732 0.360 10 87960952 stop gained C/A;G snv 14
rs10505477
CASC8 ; PCAT1 ; POU5F1B
0.658 0.400 8 127395198 intron variant A/G snv 0.40 13
rs6983267
PCAT1 ; CCAT2 ; CASC8 ; POU5F1B
0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 13
rs1224040268
PTEN
0.742 0.360 10 87931091 splice donor variant T/A;C snv 7.0E-06 12
rs80358920
BRCA2
0.732 0.400 13 32346841 stop gained C/G;T snv 12
rs1057520005
TP53
0.742 0.360 17 7673800 missense variant C/A;G snv 11
rs121913396
CTNNB1
0.732 0.200 3 41224607 missense variant A/C;G;T snv 11
rs7014346
CASC8 ; POU5F1B ; PCAT1
0.732 0.240 8 127412547 intron variant A/G snv 0.63 11
rs397507404
BRCA2
0.763 0.320 13 32370955 splice acceptor variant G/A;T snv 10
rs41293511
BRCA2
0.763 0.320 13 32363369 missense variant G/A;C snv 7.0E-06 10
rs80358893
BRCA2
0.763 0.320 13 32341011 stop gained C/G snv 10
rs80359014
BRCA2
0.763 0.320 13 32362596 missense variant A/G;T snv 10
rs80359031
BRCA2
0.763 0.320 13 32363190 missense variant A/T snv 10
rs80358807
BRCA2
0.763 0.280 13 32340146 stop gained C/T snv 9