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: rs13210132
rs13210132
4 1.000 6 31033366 intron variant A/G snv 4.3E-02 0.700 1.000 2 2009 2010
dbSNP: rs3871466
rs3871466
5 0.925 0.120 6 31015906 intron variant T/C snv 0.12 0.700 1.000 2 2009 2010
dbSNP: rs9391701
rs9391701
4 1.000 6 31015486 intron variant G/A snv 0.11 0.700 1.000 2 2009 2010
dbSNP: rs3869096
rs3869096
4 1.000 6 31016627 intron variant T/A;G snv 0.700 1.000 1 2010 2010
dbSNP: rs4713419
rs4713419
4 1.000 6 31025459 intron variant A/G snv 0.15 0.12 0.700 1.000 1 2010 2010