Source: ALL
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: rs28933690
rs28933690
XK
1 1.000 0.080 X 37728007 missense variant T/C snv 0.800 1.000 3 2001 2003
dbSNP: rs104894953
rs104894953
XK
1 1.000 0.080 X 37728068 stop gained G/A snv 0.700 0
dbSNP: rs104894954
rs104894954
XK
1 1.000 0.080 X 37728022 stop gained C/T snv 0.700 0