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: rs1555241857
rs1555241857
PDX1
2 0.925 0.120 13 27924351 missense variant A/C snv 0.700 0
dbSNP: rs193929377
rs193929377
PDX1
3 0.882 0.120 13 27920321 frameshift variant C/- delins 0.700 0
dbSNP: rs387906777
rs387906777
PDX1
4 0.851 0.120 13 27924382 missense variant A/G snv 0.700 0
dbSNP: rs80356661
rs80356661
PDX1
3 0.882 0.120 13 27924341 missense variant G/T snv 0.700 0
dbSNP: rs80356662
rs80356662
PDX1
2 0.925 0.120 13 27924381 missense variant G/A snv 0.700 0