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: rs12494623
rs12494623
1 1.000 0.080 3 179214763 intron variant C/G;T snv 0.010 1.000 1 2015 2015
dbSNP: rs3729679
rs3729679
1 1.000 0.080 3 179204642 intron variant A/G snv 0.58 0.010 1.000 1 2015 2015