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: rs12457893
rs12457893
1 1.000 0.080 18 63258928 intron variant A/C snv 0.39 0.010 1.000 1 2012 2012
dbSNP: rs8094315
rs8094315
1 1.000 0.080 18 63268814 intron variant A/G snv 0.17 0.010 1.000 1 2012 2012