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: rs10208529
rs10208529
5 0.925 0.120 2 27563321 intron variant A/T snv 0.28 0.700 1.000 2 2011 2013
dbSNP: rs1919127
rs1919127
6 0.925 0.120 2 27578626 missense variant T/C snv 0.31 0.27 0.700 1.000 2 2011 2013
dbSNP: rs1919128
rs1919128
8 0.882 0.120 2 27578892 missense variant A/G snv 0.30 0.24 0.700 1.000 2 2011 2013
dbSNP: rs4665382
rs4665382
5 0.925 0.120 2 27560934 intron variant T/C snv 0.23 0.700 1.000 2 2011 2013
dbSNP: rs4665383
rs4665383
5 0.925 0.120 2 27568688 synonymous variant C/G snv 0.24 0.700 1.000 2 2011 2013
dbSNP: rs4665991
rs4665991
5 0.925 0.120 2 27543417 intron variant G/A snv 0.24 0.700 1.000 2 2011 2013