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: rs6812193
rs6812193
3 0.882 0.080 4 76277833 intron variant C/T snv 0.38 0.880 0.667 12 2009 2017
dbSNP: rs7655536
rs7655536
1 1.000 0.040 4 76255615 intron variant T/A;C snv 0.700 1.000 1 2011 2011
dbSNP: rs7666265
rs7666265
1 1.000 0.040 4 76255128 intron variant G/A;T snv 0.700 1.000 1 2011 2011