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: rs12902958
rs12902958
7 0.807 0.080 15 69747915 intron variant G/A snv 7.7E-02 0.700 1.000 1 2017 2017
dbSNP: rs2117234
rs2117234
1 1.000 0.080 15 69746861 intron variant C/T snv 0.50 0.700 1.000 1 2017 2017
dbSNP: rs7177657
rs7177657
7 0.807 0.080 15 69749354 intron variant T/C snv 8.7E-02 0.700 1.000 1 2017 2017