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: rs11001819
rs11001819
4 10 76555466 intron variant G/A snv 0.41 0.700 1.000 1 2011 2011
dbSNP: rs2637260
rs2637260
2 10 76560588 intron variant T/C snv 0.53 0.700 1.000 1 2014 2014