Gene: PLCL2 ×
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: rs73139272
rs73139272
PLCL2
1 3 16816965 intron variant G/A;T snv 0.700 1.000 2 2018 2018
dbSNP: rs748832
rs748832
PLCL2
1 3 16809700 intron variant G/A snv 0.59 0.700 1.000 2 2017 2019
dbSNP: rs6779302
rs6779302
PLCL2
1 3 16818207 intron variant T/A;G snv 0.700 1.000 1 2017 2017
dbSNP: rs73139274
rs73139274
PLCL2
1 3 16817019 intron variant C/G snv 0.16 0.700 1.000 1 2019 2019
dbSNP: rs9846711
rs9846711
PLCL2
2 1.000 0.040 3 16821370 intron variant T/C snv 0.58 0.700 1.000 1 2019 2019