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: rs4959053
rs4959053
2 0.925 0.280 6 31131800 intron variant G/A snv 6.3E-02 0.800 1.000 2 2012 2013
dbSNP: rs3095324
rs3095324
1 1.000 0.200 6 31119356 intron variant C/T snv 0.35 0.700 1.000 1 2012 2012
dbSNP: rs386579334
rs386579334
1 1.000 0.200 6 31119356 intron variant C/T snv 0.700 1.000 1 2012 2012