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: rs12050884
rs12050884
4 15 40014133 intron variant C/A snv 0.25 0.700 1.000 2 2016 2019
dbSNP: rs12164905
rs12164905
2 15 40008490 intron variant G/T snv 0.16 0.700 1.000 1 2017 2017