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: rs1273385
rs1273385
1 16 8712564 intron variant T/C snv 0.68 0.700 1.000 1 2013 2013
dbSNP: rs1640980
rs1640980
1 16 8709764 intron variant A/C snv 0.68 0.700 1.000 1 2013 2013
dbSNP: rs1731061
rs1731061
1 16 8709147 intron variant A/G snv 0.69 0.700 1.000 1 2013 2013
dbSNP: rs1731062
rs1731062
1 16 8708895 intron variant C/T snv 0.69 0.700 1.000 1 2013 2013
dbSNP: rs1731069
rs1731069
1 16 8706975 intron variant C/A;T snv 0.700 1.000 1 2013 2013
dbSNP: rs1731070
rs1731070
1 16 8706762 intron variant G/A;C snv 0.700 1.000 1 2013 2013
dbSNP: rs3095512
rs3095512
1 16 8708187 intron variant T/A snv 0.69 0.700 1.000 1 2013 2013