Gene: PPIEL ×
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: rs4660808
rs4660808
PPIEL
3 1 39552837 intron variant C/T snv 0.17 0.700 1.000 1 2016 2016
dbSNP: rs72663520
rs72663520
PPIEL
1 1 39537738 intron variant C/T snv 0.17 0.700 1.000 1 2018 2018