Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1555657073
rs1555657073
FZD2
2 0.925 0.120 17 44558989 missense variant G/T snv 0.700 0
dbSNP: rs869025215
rs869025215
DVL3
2 0.925 0.200 3 184170088 frameshift variant G/- delins 0.700 0
dbSNP: rs869025216
rs869025216
DVL3
2 0.925 0.200 3 184170317 splice acceptor variant A/G snv 0.700 0
dbSNP: rs869025217
rs869025217
DVL3
2 0.925 0.200 3 184170318 splice acceptor variant G/A snv 0.700 0
dbSNP: rs869025218
rs869025218
DVL3
2 0.925 0.200 3 184170320 frameshift variant C/- del 0.700 0
dbSNP: rs869025219
rs869025219
DVL3
2 0.925 0.200 3 184170353 frameshift variant C/- del 0.700 0