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
rs2066827
GPR19 ; CDKN1B
0.695 0.320 12 12718165 missense variant T/A;C;G snv 1.6E-04; 1.6E-05; 0.26 21
rs121913228
CTNNB1
0.742 0.200 3 41224621 missense variant T/C;G snv 14
rs1057518903
MEN1
0.882 0.160 11 64807890 splice region variant C/- delins 6
rs1555166368
MEN1
0.851 0.120 11 64809738 frameshift variant GA/- del 6
rs1057518933
CASR
0.851 0.160 3 122284403 missense variant G/A snv 5
rs2959656
MEN1 ; MAP4K2
0.851 0.160 11 64804546 missense variant T/C snv 0.94 0.90 5
rs786202497
CHEK2
0.882 0.200 22 28719423 frameshift variant C/- del 4
rs121434265
LOC101929160 ; CDC73
0.925 0.080 1 193125142 stop gained C/G snv 3
rs374453691
PCA3 ; PRUNE2
0.925 0.080 9 76707245 missense variant C/T snv 2.0E-04 1.7E-04 2
rs768299768
POMC
0.925 0.200 2 25161505 missense variant C/A;T snv 9.2E-06 2
rs759506294
POMC
1.000 0.080 2 25161526 missense variant C/A;T snv 5.1E-06 1