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: rs4737009
rs4737009
3 1.000 0.080 8 41772887 intron variant G/A snv 0.33 0.800 1.000 2 2012 2017
dbSNP: rs10099197
rs10099197
1 8 41796940 intron variant C/T snv 0.79 0.700 1.000 1 2012 2012
dbSNP: rs149489081
rs149489081
2 8 41732218 intron variant T/G snv 5.8E-03 0.700 1.000 1 2016 2016
dbSNP: rs1579274
rs1579274
1 8 41801405 intron variant T/A;G snv 0.700 1.000 1 2012 2012
dbSNP: rs2010743
rs2010743
1 8 41816411 intron variant T/A snv 0.80 0.700 1.000 1 2012 2012
dbSNP: rs2032736
rs2032736
1 8 41781748 intron variant C/A snv 0.19 0.700 1.000 1 2012 2012
dbSNP: rs2111804
rs2111804
1 8 41786748 intron variant A/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs2111805
rs2111805
1 8 41785939 intron variant G/C;T snv 0.700 1.000 1 2012 2012
dbSNP: rs34664882
rs34664882
2 8 41686157 missense variant G/A snv 2.3E-02 2.1E-02 0.700 1.000 1 2016 2016
dbSNP: rs3758128
rs3758128
1 8 41799848 intron variant G/A snv 0.85 0.700 1.000 1 2012 2012
dbSNP: rs4466386
rs4466386
1 8 41822335 intron variant T/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs4737010
rs4737010
6 8 41772929 intron variant G/A snv 0.32 0.700 1.000 1 2016 2016
dbSNP: rs488758
rs488758
1 8 41750197 intron variant G/A snv 0.31 0.700 1.000 1 2012 2012
dbSNP: rs6999814
rs6999814
1 8 41803336 intron variant C/A snv 0.80 0.700 1.000 1 2012 2012
dbSNP: rs7461534
rs7461534
1 8 41771132 intron variant A/G snv 0.29 0.700 1.000 1 2012 2012
dbSNP: rs7823138
rs7823138
1 8 41787343 intron variant T/C snv 0.79 0.700 1.000 1 2012 2012
dbSNP: rs990174
rs990174
1 8 41774712 intron variant C/T snv 0.19 0.700 1.000 1 2012 2012