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: rs11847697
rs11847697
5 14 30045906 intron variant C/T snv 0.13 0.700 1.000 4 2010 2018
dbSNP: rs10151686
rs10151686
1 14 29997260 intron variant G/A;T snv 0.700 1.000 1 2016 2016
dbSNP: rs1191600
rs1191600
1 14 29632435 intron variant C/A snv 0.45 0.700 1.000 1 2019 2019
dbSNP: rs61980001
rs61980001
1 14 29961477 intron variant C/T snv 2.7E-02 0.700 1.000 1 2019 2019
dbSNP: rs8016859
rs8016859
1 14 30015516 intron variant G/C snv 3.2E-02 0.700 1.000 1 2019 2019