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: rs12971120
rs12971120
CNDP2
2 1.000 18 74506788 intron variant A/G snv 0.20 0.700 1.000 1 2013 2013