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: rs2075650
rs2075650
45 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 0.800 1.000 5 2008 2013
dbSNP: rs1160985
rs1160985
6 1.000 0.080 19 44900155 intron variant C/T snv 0.52 0.800 1.000 3 2013 2019
dbSNP: rs157580
rs157580
14 0.882 0.160 19 44892009 intron variant G/A snv 0.69 0.800 1.000 3 2009 2012
dbSNP: rs8106922
rs8106922
5 1.000 0.080 19 44898409 intron variant A/G snv 0.36 0.800 1.000 3 2012 2019
dbSNP: rs1038026
rs1038026
4 1.000 0.080 19 44901805 3 prime UTR variant A/G;T snv 0.700 1.000 2 2018 2019
dbSNP: rs157588
rs157588
2 19 44895007 intron variant C/T snv 0.59 0.700 1.000 1 2018 2018