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: rs142771326
rs142771326
1 1.000 0.080 11 111766340 missense variant C/G;T snv 2.0E-04 5.2E-04 0.700 0
dbSNP: rs1805076
rs1805076
7 0.851 0.120 11 111764842 missense variant C/T snv 6.5E-03 7.0E-03 0.700 0
dbSNP: rs973682124
rs973682124
1 1.000 0.080 11 111743419 missense variant T/C snv 4.0E-06 7.0E-06 0.700 0