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: rs2505901
rs2505901
SVIL ; MIR938
2 0.925 0.080 10 29602392 intron variant T/C snv 0.48 0.48 0.020 1.000 2 2012 2017