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: rs755622
rs755622
MIF ; MIF-AS1
44 0.611 0.720 22 23894205 intron variant G/C snv 0.26 0.010 1.000 1 2012 2012
dbSNP: rs773092111
rs773092111
SCYL1
1 1.000 0.040 11 65525662 missense variant G/A snv 8.1E-06 0.010 1.000 1 2017 2017