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: rs11848357
rs11848357
1 14 91038111 intron variant T/A snv 0.13 0.700 1.000 1 2014 2014
dbSNP: rs1286083
rs1286083
1 14 90976435 intron variant T/C snv 0.21 0.700 1.000 1 2012 2012