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: rs1438896
rs1438896
1 2 144888505 intron variant T/C snv 0.66 0.700 1.000 1 2017 2017
dbSNP: rs55944332
rs55944332
1 2 144969054 intron variant A/G snv 0.17 0.700 1.000 1 2017 2017
dbSNP: rs58117425
rs58117425
1 2 144924003 intron variant G/A snv 0.16 0.700 1.000 1 2017 2017
dbSNP: rs62167177
rs62167177
1 2 145181135 intron variant A/T snv 0.11 0.700 1.000 1 2017 2017