Source: INFERRED ×
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: rs12418045
rs12418045
1 1.000 0.040 11 94779904 intron variant T/C snv 4.7E-02 0.700 1.000 1 2012 2012