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: rs34064757
rs34064757
2 3 33005791 intron variant G/A snv 0.28 0.700 1.000 1 2016 2016
dbSNP: rs35480293
rs35480293
1 3 33045903 intron variant C/A snv 0.18 0.700 1.000 1 2018 2018
dbSNP: rs7646283
rs7646283
1 3 33004988 intron variant C/T snv 0.28 0.700 1.000 1 2019 2019