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: rs11144688
rs11144688
2 9 75927370 intron variant G/A snv 9.2E-02 0.700 1.000 3 2010 2014
dbSNP: rs35307904
rs35307904
1 9 75896973 intron variant G/A snv 9.8E-02 0.700 1.000 2 2019 2019
dbSNP: rs11144779
rs11144779
1 9 76177783 intron variant T/C snv 0.34 0.700 1.000 1 2019 2019
dbSNP: rs1587103
rs1587103
1 9 76250384 intron variant G/A snv 0.52 0.700 1.000 1 2019 2019
dbSNP: rs35344761
rs35344761
2 9 75895907 intron variant C/A snv 0.10 0.700 1.000 1 2017 2017
dbSNP: rs7869196
rs7869196
1 9 76141970 intron variant C/T snv 0.21 0.700 1.000 1 2019 2019