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: rs104893656
rs104893656
PAX8 ; PAX8-AS1
4 0.851 0.120 2 113246826 missense variant T/G snv 0.800 1.000 3 1998 2001
dbSNP: rs104893657
rs104893657
PAX8 ; PAX8-AS1
1 1.000 0.120 2 113246853 missense variant C/T snv 0.800 1.000 3 1998 2001
dbSNP: rs104893658
rs104893658
PAX8 ; PAX8-AS1
1 1.000 0.120 2 113246760 missense variant A/C snv 0.800 1.000 3 1998 2001
dbSNP: rs104893659
rs104893659
PAX8 ; PAX8-AS1
1 1.000 0.120 2 113246775 missense variant C/T snv 0.800 1.000 3 1998 2001
dbSNP: rs104893655
rs104893655
PAX8 ; PAX8-AS1
1 1.000 0.120 2 113244494 stop gained G/A snv 0.700 0
dbSNP: rs104893660
rs104893660
PAX8 ; PAX8-AS1
1 1.000 0.120 2 113246785 missense variant T/A;C snv 0.700 0
dbSNP: rs121917719
rs121917719
PAX8 ; PAX8-AS1
1 1.000 0.120 2 113246802 missense variant G/A snv 0.700 0