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: rs12324693
rs12324693
1 1.000 0.040 15 88200163 intron variant A/G snv 6.7E-02 0.700 1.000 1 2017 2017
dbSNP: rs16941424
rs16941424
1 1.000 0.040 15 88199729 intron variant C/G;T snv 0.700 1.000 1 2017 2017
dbSNP: rs2067559
rs2067559
1 1.000 0.040 15 88201694 intron variant A/C snv 6.7E-02 0.700 1.000 1 2017 2017
dbSNP: rs4887210
rs4887210
1 1.000 0.040 15 88210486 intron variant T/A;C snv 0.700 1.000 1 2017 2017