Source: CURATED ×
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: rs1555717982
rs1555717982
TCF4
1 1.000 0.200 18 55232601 frameshift variant A/- del 0.700 0
dbSNP: rs1555718063
rs1555718063
TCF4
1 1.000 0.200 18 55232606 stop gained C/A snv 0.700 0
dbSNP: rs1555718354
rs1555718354
TCF4
1 1.000 0.200 18 55232645 stop gained -/GACTACTG delins 0.700 0
dbSNP: rs1555718426
rs1555718426
TCF4
1 1.000 0.200 18 55232654 frameshift variant G/- del 0.700 0
dbSNP: rs1555721921
rs1555721921
TCF4
3 0.925 0.200 18 55234546 splice donor variant A/C;G snv 0.700 0
dbSNP: rs1555722023
rs1555722023
TCF4
1 1.000 0.200 18 55234565 missense variant G/C snv 0.700 0
dbSNP: rs1555764839
rs1555764839
TCF4
1 1.000 0.200 18 55254678 frameshift variant A/- delins 0.700 0
dbSNP: rs1555775233
rs1555775233
TCF4
1 1.000 0.200 18 55259950 frameshift variant -/GA delins 0.700 0
dbSNP: rs1555796785
rs1555796785
TCF4
1 1.000 0.200 18 55275649 missense variant G/C snv 0.700 0
dbSNP: rs1568331766
rs1568331766
TCF4
1 1.000 0.200 18 55232631 frameshift variant G/- del 0.700 0
dbSNP: rs1568471940
rs1568471940
TCF4
1 1.000 0.200 18 55254555 frameshift variant C/- delins 0.700 0
dbSNP: rs1568509890
rs1568509890
TCF4
1 1.000 0.200 18 55259984 frameshift variant G/- delins 0.700 0
dbSNP: rs1568523662
rs1568523662
TCF4
1 1.000 0.200 18 55261515 frameshift variant CCCGC/- delins 0.700 0
dbSNP: rs1568620706
rs1568620706
TCF4
1 1.000 0.200 18 55275665 frameshift variant AT/- delins 0.700 0
dbSNP: rs1568620774
rs1568620774
TCF4
1 1.000 0.200 18 55275667 frameshift variant -/T delins 0.700 0
dbSNP: rs1569138023
rs1569138023
TCF4
1 1.000 0.200 18 55350904 frameshift variant G/- delins 0.700 0
dbSNP: rs587784458
rs587784458
TCF4
1 1.000 0.200 18 55257314 splice donor variant C/T snv 0.700 0
dbSNP: rs587784459
rs587784459
TCF4
1 1.000 0.200 18 55232660 stop gained C/A;T snv 0.700 0
dbSNP: rs587784460
rs587784460
TCF4
1 1.000 0.200 18 55228985 missense variant C/A snv 0.700 0
dbSNP: rs587784462
rs587784462
TCF4
1 1.000 0.200 18 55228886 missense variant C/G snv 0.700 0
dbSNP: rs587784463
rs587784463
TCF4
1 1.000 0.200 18 55350958 frameshift variant G/- delins 0.700 0
dbSNP: rs587784464
rs587784464
TCF4
1 1.000 0.200 18 55350904 stop gained G/A snv 0.700 0
dbSNP: rs587784465
rs587784465
TCF4
1 1.000 0.200 18 55279550 splice donor variant C/A;T snv 0.700 0
dbSNP: rs587784466
rs587784466
TCF4
1 1.000 0.200 18 55275753 splice acceptor variant C/G snv 0.700 0
dbSNP: rs587784468
rs587784468
TCF4
1 1.000 0.200 18 55269962 frameshift variant C/- del 0.700 0