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: rs140981580
rs140981580
SSUH2
1 1.000 0.080 3 8630911 missense variant G/A;T snv 6.1E-05; 2.9E-04 0.010 1.000 1 2017 2017
dbSNP: rs4410254
rs4410254
DLX2 ; DLX2-DT
1 1.000 0.080 2 172102186 missense variant G/T snv 0.010 1.000 1 2017 2017