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: rs10908724
rs10908724
1 1 159480378 intron variant G/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs11265206
rs11265206
1 1 159479293 intron variant T/C snv 9.9E-02 0.700 1.000 1 2012 2012