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: rs121918567
rs121918567
6 0.807 0.080 6 42704609 missense variant C/A;T snv 4.0E-06 0.700 1.000 3 2003 2012
dbSNP: rs61755815
rs61755815
4 0.851 0.080 6 42704463 missense variant T/G snv 0.010 1.000 1 1996 1996
dbSNP: rs62645926
rs62645926
4 0.851 0.080 6 42721784 missense variant T/G snv 0.010 1.000 1 1996 1996
dbSNP: rs62645932
rs62645932
3 0.882 0.080 6 42704594 missense variant A/T snv 0.010 1.000 1 1996 1996