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: rs11549465
rs11549465
55 0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02 0.010 1.000 1 2012 2012
dbSNP: rs11549467
rs11549467
30 0.653 0.400 14 61740857 missense variant G/A snv 8.9E-03 7.0E-03 0.010 1.000 1 2012 2012
dbSNP: rs1430452530
rs1430452530
5 0.851 0.160 14 61721518 missense variant A/G snv 4.0E-06 0.010 1.000 1 2010 2010
dbSNP: rs2301113
rs2301113
2 0.925 0.120 14 61739830 intron variant C/A snv 0.60 0.010 1.000 1 2014 2014