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: rs35390
rs35390
SLC45A2
1 1.000 0.040 5 33955221 intron variant C/A snv 0.81 0.800 1.000 1 2011 2011