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: rs1004446
rs1004446
7 0.827 0.240 11 2148913 intron variant G/A snv 0.37 0.810 1.000 3 2007 2017
dbSNP: rs3741208
rs3741208
1 1.000 0.120 11 2148544 non coding transcript exon variant A/G;T snv 0.800 1.000 1 2007 2007
dbSNP: rs17885785
rs17885785
14 0.724 0.240 11 2146620 non coding transcript exon variant C/T snv 0.14 0.700 1.000 1 2015 2015
dbSNP: rs10770125
rs10770125
4 0.882 0.200 11 2147784 missense variant A/G snv 0.49 0.40 0.010 1.000 1 2013 2013