Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs202020308
rs202020308
TELO2
0.800 GeneticVariation UNIPROT A Syndromic Intellectual Disability Disorder Caused by Variants in TELO2, a Gene Encoding a Component of the TTT Complex. 27132593

2016
dbSNP: rs369656775
rs369656775
TELO2
0.800 GeneticVariation UNIPROT A Syndromic Intellectual Disability Disorder Caused by Variants in TELO2, a Gene Encoding a Component of the TTT Complex. 27132593

2016
dbSNP: rs371675497
rs371675497
TELO2
0.800 GeneticVariation UNIPROT A Syndromic Intellectual Disability Disorder Caused by Variants in TELO2, a Gene Encoding a Component of the TTT Complex. 27132593

2016
dbSNP: rs754162070
rs754162070
TELO2
0.800 GeneticVariation UNIPROT A Syndromic Intellectual Disability Disorder Caused by Variants in TELO2, a Gene Encoding a Component of the TTT Complex. 27132593

2016
dbSNP: rs878853271
rs878853271
TELO2
0.800 GeneticVariation UNIPROT A Syndromic Intellectual Disability Disorder Caused by Variants in TELO2, a Gene Encoding a Component of the TTT Complex. 27132593

2016
dbSNP: rs202020308
rs202020308
TELO2
T 0.800 GeneticVariation CLINVAR

dbSNP: rs202020308
rs202020308
TELO2
T 0.800 CausalMutation CLINVAR

dbSNP: rs369656775
rs369656775
TELO2
T 0.800 CausalMutation CLINVAR

dbSNP: rs371675497
rs371675497
TELO2
A 0.800 CausalMutation CLINVAR

dbSNP: rs754162070
rs754162070
TELO2
A 0.800 CausalMutation CLINVAR

dbSNP: rs878853271
rs878853271
TELO2
T 0.800 CausalMutation CLINVAR

dbSNP: rs142217951
rs142217951
TELO2
G 0.700 GeneticVariation CLINVAR