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: rs11806219
rs11806219
1 1 27121557 intron variant G/A snv 6.0E-02 0.700 1.000 1 2012 2012
dbSNP: rs11807614
rs11807614
1 1 27138426 intron variant A/G snv 1.9E-02 0.700 1.000 1 2012 2012