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: rs13058338
rs13058338
RAC2
4 1.000 0.040 22 37236730 intron variant T/A;G snv 0.010 1.000 1 2013 2013