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: rs13139571
rs13139571
9 1.000 0.040 4 155724361 intron variant C/A snv 0.22 0.700 1.000 4 2011 2018
dbSNP: rs11725969
rs11725969
5 4 155705436 intron variant C/T snv 0.24 0.700 1.000 1 2018 2018
dbSNP: rs13143871
rs13143871
3 4 155698052 intron variant T/C snv 0.25 0.700 1.000 1 2015 2015
dbSNP: rs7692387
rs7692387
5 0.925 0.080 4 155714157 intron variant G/A snv 0.16 0.700 1.000 1 2016 2016