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: rs11824953
rs11824953
3 11 102949239 intron variant C/G snv 2.7E-02 0.700 1.000 1 2012 2012
dbSNP: rs11828157
rs11828157
5 11 102947395 intron variant G/A snv 4.7E-02 0.700 1.000 1 2012 2012