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: rs10786161
rs10786161
1 1.000 0.080 10 94347914 intron variant C/T snv 0.31 0.700 1.000 1 2011 2011
dbSNP: rs10882424
rs10882424
1 1.000 0.080 10 94326321 intron variant T/G snv 0.31 0.700 1.000 1 2011 2011
dbSNP: rs10882430
rs10882430
1 1.000 0.080 10 94330915 3 prime UTR variant A/G snv 0.31 0.700 1.000 1 2011 2011
dbSNP: rs11187876
rs11187876
1 1.000 0.080 10 94330382 3 prime UTR variant C/T snv 0.31 0.700 1.000 1 2011 2011
dbSNP: rs6583937
rs6583937
1 1.000 0.080 10 94323695 intron variant A/G snv 0.32 0.700 1.000 1 2011 2011