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: rs3212220
rs3212220
1 1.000 0.040 5 159327187 intron variant C/A snv 0.26 0.010 1.000 1 2011 2011
dbSNP: rs3213094
rs3213094
2 0.925 0.080 5 159323761 intron variant C/G;T snv 0.26 0.010 1.000 1 2011 2011