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: rs6715106
rs6715106
1 1.000 0.080 2 191048308 intron variant A/G snv 6.1E-02 0.800 1.000 2 2011 2012
dbSNP: rs13401064
rs13401064
1 1.000 0.080 2 191105604 intron variant C/G snv 8.5E-02 0.700 1.000 1 2016 2016
dbSNP: rs6749371
rs6749371
2 0.925 0.200 2 191037458 intron variant A/T snv 7.3E-02 0.700 1.000 1 2016 2016
dbSNP: rs6752770
rs6752770
1 1.000 0.080 2 191108837 intron variant A/G snv 0.31 0.700 1.000 1 2011 2011