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: rs12466358
rs12466358
CHRND
1 1.000 0.080 2 232532815 intron variant T/G snv 0.22 0.010 1.000 1 2010 2010