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: rs1568305976
rs1568305976
TCF4
2 0.925 0.280 18 55229021 missense variant G/A snv 0.700 0
dbSNP: rs1568622225
rs1568622225
TCF4
2 0.925 0.280 18 55275712 frameshift variant C/- delins 0.700 0