Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4135385
CTNNB1
0.742 0.320 3 41237949 non coding transcript exon variant A/G snv 0.19 14
rs121913409
CTNNB1
0.708 0.400 3 41224646 missense variant C/A;G;T snv 13
rs121913400
CTNNB1
0.683 0.360 3 41224610 missense variant C/A;G;T snv 10
rs121913403
CTNNB1
0.683 0.240 3 41224622 missense variant C/A;G;T snv 10
rs121913412
CTNNB1
0.724 0.280 3 41224633 missense variant A/C;G;T snv 9
rs2293303
CTNNB1
0.827 0.200 3 41239336 synonymous variant C/T snv 3.2E-02 1.2E-02 7
rs28931589
CTNNB1
0.695 0.240 3 41224613 missense variant G/A;C;T snv 6
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
rs28931588
CTNNB1
0.701 0.200 3 41224606 missense variant G/A;C;T snv 5
rs121913399
CTNNB1
0.724 0.200 3 41224612 missense variant G/A;C snv 4
rs3864004
CTNNB1
0.882 0.200 3 41198686 5 prime UTR variant G/A snv 0.40 4
rs121913228
CTNNB1
0.742 0.200 3 41224621 missense variant T/C;G snv 3
rs370662884
CTNNB1
0.925 0.080 3 41225816 synonymous variant G/A snv 3.2E-05 4.9E-05 3
rs11564475
CTNNB1
0.882 0.080 3 41238542 intron variant A/G snv 3.7E-02 3
rs121913407
CTNNB1
0.763 0.240 3 41224645 missense variant T/C;G snv 3
rs2953
CTNNB1
0.925 0.040 3 41239897 3 prime UTR variant T/G snv 0.41 2
rs1798802
CTNNB1
3 41220488 intron variant A/G snv 0.43 2
rs13072632
CTNNB1
0.925 0.080 3 41220953 5 prime UTR variant T/C snv 0.41 2
rs1880481
CTNNB1
0.925 0.080 3 41230590 intron variant C/A snv 0.40 2
rs121913413
CTNNB1
0.763 0.240 3 41224634 missense variant C/A;T snv 2
rs121913396
CTNNB1
0.732 0.200 3 41224607 missense variant A/C;G;T snv 2
rs139085081
CTNNB1
1.000 0.080 3 41225436 missense variant C/T snv 1.4E-05 1
rs1057519837
CTNNB1
1.000 0.040 3 41224631 missense variant C/G;T snv 1
rs1171472831
CTNNB1
1.000 0.040 3 41224664 missense variant A/G snv 4.0E-06 1