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: rs1805410
rs1805410
PARP1
1 1.000 0.040 1 226380964 intron variant T/C snv 0.13 0.010 1.000 1 2010 2010