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: rs104893891
rs104893891
1 1.000 5 37815827 missense variant T/A;C snv 0.800 1.000 4 1996 2000
dbSNP: rs121918536
rs121918536
1 1.000 5 37815654 missense variant G/C snv 9.9E-05 1.0E-04 0.800 1.000 4 1996 2000
dbSNP: rs36119840
rs36119840
6 0.807 0.280 5 37816010 missense variant G/A snv 2.3E-03 2.7E-03 0.700 1.000 4 1996 2000
dbSNP: rs777451569
rs777451569
1 1.000 5 37834736 missense variant G/A snv 3.3E-05 6.3E-05 0.700 1.000 4 1996 2000