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: rs770689762
rs770689762
ADA2
1 1.000 0.120 22 17182696 missense variant C/T snv 3.6E-05 4.2E-05 0.700 0
dbSNP: rs775440641
rs775440641
ADA2
2 0.925 0.120 22 17188342 missense variant T/C snv 8.0E-06 0.700 0