Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913400
CTNNB1
0.683 0.360 3 41224610 missense variant C/A;G;T snv 26
rs1559470315
CTNNB1
0.732 0.320 3 41227287 protein altering variant CCACAAGCAG/T delins 26
rs121913403
CTNNB1
0.683 0.240 3 41224622 missense variant C/A;G;T snv 23
rs121913409
CTNNB1
0.708 0.400 3 41224646 missense variant C/A;G;T snv 21
rs121913412
CTNNB1
0.724 0.280 3 41224633 missense variant A/C;G;T snv 19
rs28931588
CTNNB1
0.701 0.200 3 41224606 missense variant G/A;C;T snv 17
rs28931589
CTNNB1
0.695 0.240 3 41224613 missense variant G/A;C;T snv 17
rs121913228
CTNNB1
0.742 0.200 3 41224621 missense variant T/C;G snv 14
rs4135385
CTNNB1
0.742 0.320 3 41237949 non coding transcript exon variant A/G snv 0.19 14
rs121913396
CTNNB1
0.732 0.200 3 41224607 missense variant A/C;G;T snv 13
rs121913399
CTNNB1
0.724 0.200 3 41224612 missense variant G/A;C snv 13
rs121913407
CTNNB1
0.763 0.240 3 41224645 missense variant T/C;G snv 12
rs1057519886
CTNNB1
0.752 0.240 3 41224609 missense variant T/A;C;G snv 11
rs121913413
CTNNB1
0.763 0.240 3 41224634 missense variant C/A;T snv 11
rs775104326
CTNNB1
0.776 0.160 3 41224995 stop gained C/A;T snv 4.0E-06 10
rs1553630279
CTNNB1
0.807 0.160 3 41225049 stop gained C/T snv 7
rs2293303
CTNNB1
0.827 0.200 3 41239336 synonymous variant C/T snv 3.2E-02 1.2E-02 7
rs4533622
CTNNB1
0.807 0.240 3 41200847 intron variant C/A;T snv 6
rs1233296947
CTNNB1
0.851 0.080 3 41225746 missense variant G/A snv 4.0E-06 5
rs1553632357
CTNNB1
0.882 0.120 3 41236421 stop gained G/T snv 5
rs1553631770
CTNNB1
1.000 3 41233398 missense variant A/T snv 4
rs3864004
CTNNB1
0.882 0.200 3 41198686 5 prime UTR variant G/A snv 0.40 4
rs1057519379
CTNNB1
0.882 0.080 3 41233777 frameshift variant -/C ins 3
rs11564475
CTNNB1
0.882 0.080 3 41238542 intron variant A/G snv 3.7E-02 3
rs370662884
CTNNB1
0.925 0.080 3 41225816 synonymous variant G/A snv 3.2E-05 4.9E-05 3