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: rs187238
rs187238
48 0.602 0.680 11 112164265 intron variant C/A;G snv 0.030 0.333 3 2012 2015
dbSNP: rs1946518
rs1946518
46 0.602 0.760 11 112164735 intron variant T/G snv 0.60 0.030 0.667 3 2012 2015
dbSNP: rs360719
rs360719
7 0.790 0.480 11 112165426 non coding transcript exon variant A/G snv 0.25 0.030 1.000 3 2011 2015
dbSNP: rs549908
rs549908
10 0.752 0.440 11 112150193 synonymous variant T/A;G snv 4.2E-06; 0.29 0.030 1.000 3 2009 2019