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: rs7023329
rs7023329
9 0.790 0.160 9 21816529 intron variant A/G snv 0.50 0.810 1.000 5 2009 2017
dbSNP: rs10757257
rs10757257
3 0.882 0.080 9 21806565 intron variant G/A snv 0.34 0.710 1.000 2 2009 2012
dbSNP: rs201131773
rs201131773
1 1.000 0.040 9 21805207 intron variant -/AC delins 0.700 1.000 1 2017 2017
dbSNP: rs7023954
rs7023954
2 0.925 0.040 9 21816759 missense variant G/A snv 0.40 0.42 0.010 1.000 1 2016 2016
dbSNP: rs869329
rs869329
4 0.851 0.080 9 21804694 intron variant A/G;T snv 0.010 1.000 1 2019 2019
dbSNP: rs869330
rs869330
2 0.925 0.080 9 21804618 intron variant A/G snv 0.62 0.010 1.000 1 2019 2019