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: rs11730235
rs11730235
1 4 26922822 intron variant G/T snv 0.26 0.700 1.000 1 2011 2011
dbSNP: rs6844153
rs6844153
1 4 26942692 intron variant C/T snv 0.17 0.700 1.000 1 2011 2011