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: rs210134
rs210134
2 1.000 0.120 6 33572432 intron variant A/G snv 0.72 0.800 1.000 3 2011 2019
dbSNP: rs513349
rs513349
2 1.000 0.120 6 33573942 intron variant A/G snv 0.51 0.51 0.800 1.000 1 2013 2019