Gene: TNRC6B ×
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: rs12484776
rs12484776
TNRC6B
2 1.000 22 40256869 intron variant A/G snv 0.19 0.700 1.000 1 2011 2011
dbSNP: rs12484951
rs12484951
TNRC6B
2 1.000 22 40307071 intron variant T/G snv 0.20 0.700 1.000 1 2018 2018
dbSNP: rs3830738
rs3830738
TNRC6B
2 1.000 22 40315223 intron variant -/T delins 0.22 0.700 1.000 1 2019 2019
dbSNP: rs4402860
rs4402860
TNRC6B
2 1.000 22 40158441 intron variant A/G;T snv 0.17 0.700 1.000 1 2018 2018
dbSNP: rs4821939
rs4821939
TNRC6B
2 1.000 22 40263247 intron variant T/A snv 0.20 0.700 1.000 1 2019 2019