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: rs193922355
rs193922355
PDX1
1 1.000 0.080 13 27924291 missense variant C/A;G snv 8.1E-06 0.700 0
dbSNP: rs193922356
rs193922356
PDX1
1 1.000 0.080 13 27924420 missense variant A/C snv 0.700 0
dbSNP: rs193922360
rs193922360
PDX1
1 1.000 0.080 13 27924622 missense variant A/G snv 7.0E-06 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