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: rs6576618
rs6576618
1 1.000 15 26799458 intron variant A/C snv 0.59 0.010 1.000 1 2013 2013
dbSNP: rs981778
rs981778
1 1.000 15 26712093 intron variant G/A snv 0.32 0.010 1.000 1 2013 2013