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: rs10405652
rs10405652
1 1.000 0.080 19 9630447 intron variant G/T snv 0.13 0.700 1.000 1 2013 2013
dbSNP: rs10411082
rs10411082
1 1.000 0.080 19 9630540 intron variant G/A snv 0.31 0.700 1.000 1 2013 2013