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: rs10828725
rs10828725
2 10 24929314 intron variant G/T snv 0.26 0.700 1.000 1 2016 2016
dbSNP: rs11014296
rs11014296
1 10 24913109 intron variant C/T snv 0.26 0.700 1.000 1 2016 2016