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: rs1052486
rs1052486
1 0.851 0.200 6 31642909 missense variant A/G snv 0.51 0.44 0.700 1.000 1 2007 2007
dbSNP: rs1077393
rs1077393
3 0.882 0.200 6 31642752 non coding transcript exon variant A/G snv 0.44 0.700 1.000 1 2007 2007
dbSNP: rs3117582
rs3117582
6 0.716 0.440 6 31652743 intron variant T/G snv 7.1E-02 0.700 1.000 1 2007 2007
dbSNP: rs3117583
rs3117583
3 0.925 0.200 6 31651799 5 prime UTR variant A/G snv 0.14 0.17 0.700 1.000 1 2007 2007
dbSNP: rs3130048
rs3130048
2 1.000 0.120 6 31645962 intron variant T/C snv 0.23 0.700 1.000 1 2007 2007
dbSNP: rs3130050
rs3130050
3 0.882 0.240 6 31650984 intron variant G/A snv 0.89 0.700 1.000 1 2007 2007
dbSNP: rs3130617
rs3130617
2 0.925 0.200 6 31659746 missense variant C/T snv 0.79 0.74 0.700 1.000 1 2007 2007