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: rs17833380
rs17833380
1 1.000 0.080 14 58917038 intron variant C/T snv 0.15 0.700 1.000 1 2009 2009
dbSNP: rs311844
rs311844
1 1.000 0.080 14 58672253 intron variant G/T snv 0.19 0.700 1.000 1 2009 2009