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: rs6737500
rs6737500
1 2 32038018 intron variant C/T snv 0.43 0.700 1.000 1 2014 2014
dbSNP: rs6748621
rs6748621
1 2 32037132 intron variant T/C snv 0.43 0.700 1.000 1 2014 2014