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: rs749663315
rs749663315
1 1.000 0.040 20 25077778 missense variant C/A;G snv 6.5E-06; 1.9E-05 0.700 0
dbSNP: rs771561481
rs771561481
2 0.925 0.040 20 25078931 missense variant C/G;T snv 4.0E-06; 1.2E-05 0.700 0
dbSNP: rs74315432
rs74315432
2 0.925 0.040 20 25079443 missense variant G/A;T snv 2.0E-05; 3.6E-05 0.800 1.000 6 2002 2011