Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs149709822
KLK3
0.882 0.080 19 50856335 missense variant G/A snv 4.0E-05 2.3E-04 4
rs17632542
KLK3
0.925 0.080 19 50858501 missense variant T/C snv 5.5E-02 4.9E-02 4
rs266882
KLK3
0.925 0.080 19 50854757 upstream gene variant G/A snv 0.49 4
rs765521022
KLK3
0.851 0.080 19 50858171 missense variant T/C snv 4
rs1450063773
KLK3
0.925 0.080 19 50858491 missense variant C/A;T snv 8.0E-06; 4.0E-06 3
rs538660698
KLK3
0.882 0.200 19 50860077 missense variant G/A;T snv 8.0E-06 3
rs1058205
KLK3
0.925 0.080 19 50860142 3 prime UTR variant C/T snv 0.75 0.74 2
rs1192131078
KLK3
0.925 0.080 19 50858075 missense variant G/A snv 4.0E-06 2
rs141576693
KLK3
0.925 0.080 19 50856263 missense variant C/T snv 8.0E-05 2.8E-04 2
rs369223448
KLK3
0.925 0.080 19 50856347 missense variant G/A snv 3.6E-05 1.4E-05 2
rs61752561
KLK3
0.925 0.080 19 50858126 missense variant G/A snv 2.4E-02 2.5E-02 2
rs62113212
KLK3
0.925 0.080 19 50857584 non coding transcript exon variant C/G;T snv 2
rs62113214
KLK3
0.925 0.080 19 50859281 intron variant T/G snv 4.9E-02 2
rs746367915
KLK3
0.925 0.080 19 50860089 missense variant C/T snv 8.0E-06 2.8E-05 2
rs781327047
KLK3
0.925 0.080 19 50856344 missense variant G/A;C snv 4.0E-06; 4.0E-06 2