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: rs11881955
rs11881955
2 19 17143698 intron variant A/G snv 0.49 0.700 1.000 1 2017 2017
dbSNP: rs35365035
rs35365035
2 19 17141341 intron variant T/C snv 0.49 0.700 1.000 1 2016 2016
dbSNP: rs4808579
rs4808579
2 19 17144924 intron variant T/A;C snv 0.700 1.000 1 2019 2019
dbSNP: rs59616136
rs59616136
4 19 17141231 intron variant G/A snv 8.1E-02 0.700 1.000 1 2016 2016