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: rs62635004
rs62635004
2 0.925 0.080 X 38297391 missense variant C/T snv 0.010 1.000 1 2006 2006
dbSNP: rs62638634
rs62638634
4 0.925 0.080 X 38322921 missense variant C/A snv 0.010 1.000 1 1998 1998
dbSNP: rs62642057
rs62642057
3 0.882 0.080 X 38304746 missense variant C/T snv 0.010 1.000 1 2007 2007