Gene: TRIM66 ×
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: rs4256980
rs4256980
TRIM66
2 11 8652392 intron variant C/G snv 0.59 0.700 1.000 3 2015 2019
dbSNP: rs4929923
rs4929923
TRIM66
3 11 8617653 3 prime UTR variant T/C snv 0.59 0.700 1.000 3 2017 2019
dbSNP: rs10840100
rs10840100
TRIM66
2 11 8647890 intron variant A/G snv 0.59 0.700 1.000 2 2015 2018
dbSNP: rs10840099
rs10840099
TRIM66
1 11 8646133 intron variant T/C snv 0.59 0.700 1.000 1 2017 2017
dbSNP: rs11042023
rs11042023
TRIM66
3 1.000 0.080 11 8640969 missense variant T/C snv 0.60 0.59 0.700 1.000 1 2018 2018
dbSNP: rs7113874
rs7113874
TRIM66
2 11 8666469 intron variant C/T snv 0.42 0.700 1.000 1 2017 2017