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: rs11072566
rs11072566
5 0.925 0.120 15 76001630 intron variant A/G snv 0.45 0.700 1.000 1 2017 2017
dbSNP: rs11072567
rs11072567
5 15 76006403 intron variant A/G snv 0.43 0.700 1.000 1 2016 2016
dbSNP: rs74024059
rs74024059
2 15 76010569 intron variant C/G;T snv 3.9E-02 0.700 1.000 1 2016 2016