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: rs10490924
rs10490924
ARMS2 ; LOC105378525
16 0.716 0.240 10 122454932 missense variant G/T snv 0.26 0.23 0.010 1.000 1 2011 2011
dbSNP: rs281865250
rs281865250
BEST1 ; LOC107984334
2 0.925 0.080 11 61959507 missense variant C/A snv 0.010 1.000 1 2011 2011