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: rs10762524
rs10762524
PRKG1
1 1.000 0.040 10 52014152 intron variant T/A;C;G snv 0.700 1.000 1 2010 2010