Source: ALL
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: rs12451939
rs12451939
MED13
1 1.000 0.120 17 61970281 intron variant A/G snv 2.6E-02 0.700 1.000 1 2011 2011