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: rs10774214
rs10774214
9 0.790 0.080 12 4259186 intron variant T/C snv 0.54 0.700 1.000 4 2013 2019
dbSNP: rs12818766
rs12818766
9 0.790 0.080 12 4266925 intron variant G/A snv 0.17 0.700 1.000 1 2019 2019
dbSNP: rs35808169
rs35808169
10 0.776 0.080 12 4259441 intron variant T/C snv 0.17 0.700 1.000 1 2019 2019
dbSNP: rs4572213
rs4572213
9 0.790 0.080 12 4256383 intron variant A/T snv 0.10 0.700 1.000 1 2018 2018