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: rs2061174
rs2061174
3 0.882 0.080 7 136976653 intron variant G/A;C snv 0.010 1.000 1 2004 2004
dbSNP: rs324650
rs324650
5 0.827 0.080 7 137008914 intron variant T/A snv 0.55 0.010 1.000 1 2004 2004
dbSNP: rs1217691063
rs1217691063
614 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 0.010 1.000 1 2009 2009