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: rs17473118
rs17473118
1 3 43402042 intron variant G/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs7650267
rs7650267
1 3 43426403 intron variant T/C snv 0.15 0.700 1.000 1 2012 2012