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: rs1565430886
rs1565430886
1 11 77189430 missense variant T/C snv 0.700 0
dbSNP: rs1565469959
rs1565469959
1 11 77203220 splice region variant A/G snv 0.700 0
dbSNP: rs192378817
rs192378817
1 11 77183146 missense variant C/A;T snv 3.9E-05 1.5E-04 0.700 0
dbSNP: rs746667217
rs746667217
1 11 77205503 missense variant C/G;T snv 6.4E-05 2.1E-05 0.700 0
dbSNP: rs751242455
rs751242455
1 11 77204094 missense variant G/A;C snv 8.8E-06; 4.4E-05 0.700 0