Gene: TRIM33 ×
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: rs11102800
rs11102800
TRIM33
2 1.000 0.040 1 114498310 intron variant C/T snv 0.58 0.800 1.000 1 2014 2014
dbSNP: rs11582563
rs11582563
TRIM33
1 1.000 0.040 1 114416918 intron variant G/A snv 0.14 0.800 1.000 1 2014 2014
dbSNP: rs11585926
rs11585926
TRIM33
3 1.000 0.040 1 114431068 intron variant T/C snv 0.22 0.800 1.000 1 2014 2014
dbSNP: rs11589568
rs11589568
TRIM33
1 1.000 0.040 1 114453702 intron variant T/C snv 0.14 0.800 1.000 1 2014 2014
dbSNP: rs3827735
rs3827735
TRIM33
1 1.000 0.040 1 114510087 intron variant C/A;T snv 0.800 1.000 1 2014 2014
dbSNP: rs6537825
rs6537825
TRIM33
1 1.000 0.040 1 114405659 missense variant A/G snv 0.88 0.92 0.800 1.000 1 2014 2014
dbSNP: rs6661053
rs6661053
TRIM33
1 1.000 0.040 1 114496497 intron variant T/A;C snv 0.800 1.000 1 2014 2014
dbSNP: rs7511633
rs7511633
TRIM33
1 1.000 0.040 1 114456655 intron variant G/A snv 0.36 0.800 1.000 1 2014 2014