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: rs13098327
rs13098327
2 3 85771031 intron variant G/A snv 0.15 0.700 1.000 1 2015 2015
dbSNP: rs9813495
rs9813495
4 3 85777231 intron variant A/G snv 0.15 0.700 1.000 1 2017 2017