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: rs1456314
rs1456314
PCAT1
1 1.000 0.080 8 127063445 intron variant A/G snv 0.64 0.700 1.000 1 2007 2007