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: rs1044498
rs1044498
15 0.752 0.360 6 131851228 missense variant A/C;G snv 0.19 0.100 0.800 10 2009 2019
dbSNP: rs1799774
rs1799774
3 0.882 0.200 6 131882331 intron variant T/- delins 0.010 1.000 1 2006 2006
dbSNP: rs2021966
rs2021966
2 1.000 0.080 6 131829299 intron variant A/G snv 0.42 0.010 1.000 1 2008 2008
dbSNP: rs55725924
rs55725924
1 1.000 0.080 6 131894348 3 prime UTR variant T/A;C snv 0.010 1.000 1 2017 2017
dbSNP: rs7754561
rs7754561
3 0.882 0.200 6 131891554 3 prime UTR variant A/G snv 0.44 0.010 1.000 1 2006 2006
dbSNP: rs7754586
rs7754586
1 1.000 0.080 6 131891602 3 prime UTR variant A/C snv 0.30 0.010 1.000 1 2017 2017
dbSNP: rs943003
rs943003
3 0.882 0.120 6 131819872 non coding transcript exon variant C/T snv 0.64 0.010 1.000 1 2008 2008
dbSNP: rs997509
rs997509
6 0.827 0.200 6 131846837 intron variant C/T snv 5.3E-02 0.010 1.000 1 2006 2006