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: rs9883204
rs9883204
1 3 123377973 intron variant T/A;C snv 0.800 1.000 2 2010 2013
dbSNP: rs11708067
rs11708067
9 0.882 0.080 3 123346931 intron variant A/G snv 0.19 0.700 1.000 1 2019 2019
dbSNP: rs11719201
rs11719201
1 3 123349897 intron variant C/T snv 0.20 0.700 1.000 1 2016 2016
dbSNP: rs9851257
rs9851257
1 3 123406864 intron variant T/A snv 0.33 0.700 1.000 1 2019 2019