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: rs1743963
rs1743963
4 0.882 0.120 6 134176537 intron variant G/A;C snv 0.010 1.000 1 2019 2019
dbSNP: rs1763509
rs1763509
4 0.882 0.120 6 134233200 intron variant G/A;T snv 0.010 1.000 1 2019 2019
dbSNP: rs9376026
rs9376026
3 0.925 0.080 6 134281316 intron variant T/C snv 0.43 0.010 1.000 1 2019 2019
dbSNP: rs9389154
rs9389154
4 0.882 0.120 6 134293623 intron variant G/A snv 0.11 0.010 1.000 1 2019 2019