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: rs12521097
rs12521097
1 1.000 0.040 5 132239645 intron variant G/A snv 0.42 0.700 1.000 1 2007 2007
dbSNP: rs3844312
rs3844312
1 1.000 0.040 5 132246663 intron variant C/T snv 0.34 0.700 1.000 1 2007 2007