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: rs1505307
rs1505307
7 3 24301839 intron variant T/C snv 0.60 0.700 1.000 2 2017 2018
dbSNP: rs113700287
rs113700287
4 3 24293020 intron variant -/GTT delins 0.700 1.000 1 2016 2016
dbSNP: rs1349265
rs1349265
3 1.000 0.040 3 24117896 3 prime UTR variant A/C;G snv 0.700 1.000 1 2019 2019
dbSNP: rs3749376
rs3749376
1 3 24496776 non coding transcript exon variant G/C;T snv 0.700 1.000 1 2019 2019
dbSNP: rs869784
rs869784
3 3 24306517 intron variant T/C snv 0.68 0.700 1.000 1 2019 2019
dbSNP: rs9310736
rs9310736
4 3 24309320 intron variant A/G snv 0.69 0.700 1.000 1 2010 2010