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: rs1256062
rs1256062
2 0.925 0.120 14 64236600 intron variant T/C snv 0.21 0.010 1.000 1 2007 2007
dbSNP: rs1271572
rs1271572
16 0.708 0.400 14 64295199 intron variant A/C;T snv 0.010 1.000 1 2007 2007
dbSNP: rs944050
rs944050
5 0.827 0.280 14 64233327 splice region variant T/C snv 9.5E-02 7.9E-02 0.010 1.000 1 2016 2016