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: rs10180371
rs10180371
1 2 205150255 intron variant A/G snv 0.64 0.700 1.000 1 2018 2018
dbSNP: rs16837021
rs16837021
1 2 205138311 intron variant C/T snv 0.22 0.700 1.000 1 2018 2018
dbSNP: rs73057184
rs73057184
1 2 205110118 intron variant C/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs7560015
rs7560015
1 2 205141917 intron variant C/A;T snv 0.700 1.000 1 2018 2018