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: rs17023459
rs17023459
1 2 100067088 intron variant C/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs17782474
rs17782474
1 2 99649474 intron variant A/G snv 6.6E-02 0.700 1.000 1 2018 2018
dbSNP: rs2309757
rs2309757
1 2 100191263 intron variant T/C snv 0.29 0.700 1.000 1 2018 2018
dbSNP: rs6709656
rs6709656
1 2 100190257 intron variant A/G snv 0.29 0.700 1.000 1 2018 2018