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: rs12603526
rs12603526
NXN
9 0.790 0.080 17 897353 intron variant T/C snv 2.3E-02 0.700 1.000 2 2014 2016
dbSNP: rs4968127
rs4968127
NXN
10 0.776 0.080 17 906403 intron variant G/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs73975586
rs73975586
10 0.776 0.080 17 911003 non coding transcript exon variant A/T snv 9.8E-02 0.700 1.000 1 2019 2019
dbSNP: rs73975588
rs73975588
NXN
9 0.790 0.080 17 913501 intron variant A/C snv 9.9E-02 0.700 1.000 1 2019 2019