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: rs143410069
rs143410069
1 3 124554316 intron variant T/C snv 1.5E-04 0.700 1.000 1 2015 2015
dbSNP: rs151058966
rs151058966
1 3 124556840 intron variant C/G snv 1.5E-04 0.700 1.000 1 2015 2015
dbSNP: rs192210795
rs192210795
1 3 124201267 intron variant G/A;T snv 0.700 1.000 1 2015 2015