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: rs12027135
rs12027135
3 1 25449242 intron variant A/T snv 0.50 0.800 1.000 2 2010 2018
dbSNP: rs10903129
rs10903129
2 1 25442446 intron variant A/G snv 0.58 0.800 1.000 1 2009 2018