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: rs17356664
rs17356664
1 19 45237513 intron variant C/T snv 0.28 0.800 1.000 1 2011 2011
dbSNP: rs11083766
rs11083766
2 19 45212232 intron variant T/C snv 0.26 0.700 1.000 1 2016 2016