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: rs11047102
rs11047102
2 0.925 0.160 12 23793212 intron variant C/T snv 7.9E-02 0.800 1.000 1 2011 2011