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: rs1041981
rs1041981
25 0.667 0.520 6 31573007 missense variant C/A snv 0.35 0.38 0.720 1.000 2 2005 2007
dbSNP: rs909253
rs909253
34 0.641 0.600 6 31572536 intron variant A/G;T snv 0.700 0
dbSNP: rs1800683
rs1800683
6 0.807 0.240 6 31572294 5 prime UTR variant G/A;C snv 0.39 0.010 1.000 1 2007 2007