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: rs875989846
rs875989846
GTF2E2
2 0.925 0.080 8 30612400 missense variant C/G snv 0.800 0
dbSNP: rs875989847
rs875989847
GTF2E2
2 0.925 0.080 8 30607141 missense variant C/A snv 0.800 0