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: rs202247806
rs202247806
SLC25A15
3 1.000 0.160 13 40793270 missense variant C/A;T snv 4.0E-06 0.010 1.000 1 2014 2014
dbSNP: rs765136006
rs765136006
ORC1
2 1 52402180 missense variant G/A snv 2.0E-05 0.010 1.000 1 2014 2014