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: rs5749111
rs5749111
2 22 30498956 intron variant T/A snv 0.23 0.700 1.000 1 2017 2017
dbSNP: rs7287943
rs7287943
2 22 30496568 intron variant C/A;G snv 0.700 1.000 1 2019 2019
dbSNP: rs9608946
rs9608946
2 22 30496268 intron variant A/G snv 0.23 0.700 1.000 1 2016 2016