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: rs2535629
rs2535629
9 0.827 0.040 3 52799203 intron variant G/A;C snv 0.700 1.000 1 2013 2013
dbSNP: rs3617
rs3617
3 1.000 0.040 3 52799789 missense variant C/A snv 0.48 0.54 0.700 1.000 1 2017 2017