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: rs6870983
rs6870983
3 5 88401716 intron variant C/T snv 0.29 0.700 1.000 4 2015 2018
dbSNP: rs7444298
rs7444298
1 5 88434210 non coding transcript exon variant A/G snv 0.31 0.700 1.000 1 2019 2019