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: rs2479106
rs2479106
4 0.851 0.120 9 123762933 intron variant A/G snv 0.44 0.900 0.833 12 2011 2019
dbSNP: rs10818854
rs10818854
6 0.851 0.200 9 123684499 intron variant G/A snv 5.7E-02 0.830 1.000 4 2011 2018
dbSNP: rs10986105
rs10986105
2 0.925 0.200 9 123787676 intron variant T/G snv 6.9E-02 0.730 1.000 4 2011 2018
dbSNP: rs1627536
rs1627536
1 1.000 0.120 9 123780425 intron variant A/G;T snv 0.700 1.000 1 2011 2011
dbSNP: rs1778890
rs1778890
1 1.000 0.120 9 123769476 intron variant T/C snv 0.25 0.35 0.700 1.000 1 2011 2011
dbSNP: rs7857605
rs7857605
1 1.000 0.120 9 123745334 intron variant T/C snv 7.5E-02 0.700 1.000 1 2011 2011
dbSNP: rs9696009
rs9696009
1 1.000 0.120 9 123856954 intron variant G/A snv 0.17 0.700 1.000 1 2018 2018
dbSNP: rs189947178
rs189947178
1 1.000 0.120 9 123382111 missense variant G/T snv 5.1E-03 5.0E-03 0.010 1.000 1 2013 2013