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: rs10239940
rs10239940
2 7 73487060 intron variant A/T snv 2.6E-02 0.700 1.000 1 2012 2012
dbSNP: rs13244268
rs13244268
5 0.925 0.120 7 73497513 intron variant T/C snv 9.2E-02 0.700 1.000 1 2016 2016
dbSNP: rs2074755
rs2074755
20 0.807 0.240 7 73462836 non coding transcript exon variant T/C snv 9.2E-02 0.700 1.000 1 2016 2016
dbSNP: rs7811265
rs7811265
7 0.925 0.120 7 73520180 intron variant A/G snv 0.23 0.700 1.000 1 2018 2018