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: rs3922844
rs3922844
3 3 38582762 intron variant T/C snv 0.61 0.800 1.000 4 2011 2019
dbSNP: rs11708996
rs11708996
6 0.925 0.120 3 38592432 intron variant G/C snv 0.11 0.800 1.000 3 2010 2019
dbSNP: rs6599222
rs6599222
1 3 38606571 intron variant C/T snv 0.80 0.800 1.000 2 2011 2019
dbSNP: rs6763048
rs6763048
1 3 38639903 intron variant A/G snv 0.16 0.800 1.000 1 2012 2012
dbSNP: rs12053903
rs12053903
2 3 38551902 intron variant T/C snv 0.49 0.700 1.000 1 2010 2010
dbSNP: rs45567533
rs45567533
1 3 38630069 non coding transcript exon variant A/G snv 0.14 0.700 1.000 1 2018 2018
dbSNP: rs7374004
rs7374004
1 3 38584218 intron variant A/T snv 0.33 0.700 1.000 1 2018 2018