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: rs112916054
rs112916054
1 17 32797244 intron variant C/T snv 0.14 0.700 1.000 1 2016 2016
dbSNP: rs17183628
rs17183628
1 17 32857613 intron variant T/C snv 0.14 0.700 1.000 1 2016 2016
dbSNP: rs17780981
rs17780981
1 17 32792019 intron variant A/G snv 0.14 0.700 1.000 1 2016 2016
dbSNP: rs62070183
rs62070183
1 17 32837349 intron variant T/C snv 0.14 0.700 1.000 1 2016 2016