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: rs12716080
rs12716080
3 0.882 0.040 5 11166836 intron variant G/T snv 0.39 0.010 < 0.001 1 2011 2011
dbSNP: rs6885224
rs6885224
3 0.882 0.040 5 11169833 intron variant C/A;T snv 0.010 < 0.001 1 2011 2011