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: rs13019227
rs13019227
2 2 137168337 intron variant A/G snv 4.5E-02 0.700 1.000 1 2015 2015
dbSNP: rs550612
rs550612
1 2 136893930 intron variant C/A snv 0.66 0.700 1.000 1 2019 2019
dbSNP: rs6720647
rs6720647
1 2 136858118 intron variant A/G snv 0.13 0.700 1.000 1 2019 2019