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: rs12910178
rs12910178
CEP152
1 1.000 0.040 15 48696754 regulatory region variant C/T snv 0.70 0.700 1.000 1 2011 2011