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: rs146895361
rs146895361
1 6 51824798 intron variant G/A snv 1.7E-03 0.700 1.000 1 2015 2015
dbSNP: rs149476743
rs149476743
1 6 51770381 intron variant C/T snv 1.6E-03 0.700 1.000 1 2015 2015
dbSNP: rs150576801
rs150576801
1 6 51819190 intron variant C/T snv 1.7E-03 0.700 1.000 1 2015 2015