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: rs1049353
rs1049353
26 0.657 0.464 6 88143916 synonymous variant C/T snp 0.21 0.20 0.010 1.000 1 2012 2012
dbSNP: rs12938031
rs12938031
1 1.000 0.107 17 45777136 intron variant A/G snp 0.24 0.010 1.000 1 2011 2011
dbSNP: rs4680
rs4680
155 0.484 0.821 22 19963748 missense variant G/A snp 0.46 0.45 0.010 1.000 1 2009 2009
dbSNP: rs5522
rs5522
15 0.734 0.286 4 148436323 missense variant C/T snp 0.88 0.89 0.010 1.000 1 2010 2010