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: rs2070895
rs2070895
15 0.807 0.120 15 58431740 intron variant G/A snv 0.33 0.710 1.000 1 2008 2008
dbSNP: rs6078
rs6078
3 0.882 0.120 15 58541794 missense variant G/A;T snv 7.1E-02; 8.0E-06 0.010 1.000 1 2018 2018
dbSNP: rs6083
rs6083
1 1.000 0.080 15 58545811 missense variant A/C;G snv 4.0E-06; 0.47 0.010 1.000 1 2018 2018