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: rs6265
rs6265
272 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 0.700 1.000 7 2009 2019
dbSNP: rs11030104
rs11030104
12 0.790 0.240 11 27662970 intron variant A/G snv 0.16 0.700 1.000 6 2014 2019
dbSNP: rs2049045
rs2049045
3 1.000 0.080 11 27672694 intron variant G/A;C snv 0.13 0.700 1.000 2 2017 2019
dbSNP: rs10501087
rs10501087
1 11 27648561 intron variant T/C snv 0.17 0.700 1.000 1 2017 2017
dbSNP: rs10767654
rs10767654
2 11 27618676 intron variant T/G snv 0.73 0.700 1.000 1 2017 2017
dbSNP: rs11030100
rs11030100
2 1.000 0.080 11 27656039 3 prime UTR variant G/T snv 0.17 0.700 1.000 1 2017 2017
dbSNP: rs11030102
rs11030102
2 11 27660049 non coding transcript exon variant C/G snv 0.19 0.700 1.000 1 2017 2017
dbSNP: rs16917237
rs16917237
3 11 27680836 intron variant G/T snv 0.16 0.700 1.000 1 2015 2015
dbSNP: rs4923460
rs4923460
3 11 27635242 intron variant G/T snv 0.20 0.700 1.000 1 2017 2017
dbSNP: rs7103411
rs7103411
15 0.752 0.160 11 27678578 intron variant C/T snv 0.82 0.700 1.000 1 2017 2017
dbSNP: rs925946
rs925946
9 0.882 0.120 11 27645655 intron variant T/G snv 0.72 0.700 1.000 1 2009 2009