Gene: TRIM26 ×
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: rs116408368
rs116408368
TRIM26
2 1.000 0.040 6 30202733 intron variant T/C snv 0.700 1.000 1 2017 2017
dbSNP: rs2021722
rs2021722
TRIM26
5 0.851 0.040 6 30206354 intron variant C/A;T snv 0.24 0.700 1.000 1 2013 2013