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: rs1516725
rs1516725
8 0.925 0.120 3 186106215 intron variant T/C snv 0.86 0.700 1.000 7 2013 2019
dbSNP: rs10513801
rs10513801
3 3 186104564 intron variant T/G snv 9.2E-02 0.700 1.000 1 2019 2019
dbSNP: rs4234589
rs4234589
2 3 186101093 intron variant A/G snv 0.13 0.700 1.000 1 2017 2017
dbSNP: rs6809651
rs6809651
4 3 186096853 intron variant G/A snv 0.14 0.700 1.000 1 2017 2017
dbSNP: rs73052033
rs73052033
1 3 186110676 intron variant T/C snv 0.15 0.700 1.000 1 2019 2019