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: rs104894943
rs104894943
TBX22
2 0.925 0.120 X 80026849 missense variant C/T snv 0.700 0
dbSNP: rs104894944
rs104894944
TBX22
2 0.925 0.120 X 80023236 missense variant G/T snv 0.700 0
dbSNP: rs104894945
rs104894945
TBX22
1 1.000 0.120 X 80022435 stop gained G/C;T snv 1.5E-05 0.700 0
dbSNP: rs104894946
rs104894946
TBX22
2 0.925 0.120 X 80026711 missense variant T/C snv 0.700 0
dbSNP: rs28935177
rs28935177
TBX22
2 0.925 0.120 X 80026860 missense variant A/T snv 0.700 0