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: rs2315008
rs2315008
2 0.925 0.120 20 63712604 intron variant T/G snv 0.70 0.800 1.000 1 2008 2008
dbSNP: rs6062504
rs6062504
3 0.925 0.040 20 63717555 intron variant A/G;T snv 0.800 1.000 1 2012 2012