TELO2, telomere maintenance 2, 9894

N. diseases: 37; N. variants: 7
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs202020308
rs202020308
Entrez Id: 9894
Gene Symbol: TELO2
TELO2
CUI: C4310778
Disease:
YOU-HOOVER-FONG SYNDROME 		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
Entrez Id: 9894
Gene Symbol: TELO2
TELO2
CUI: C4310778
Disease:
YOU-HOOVER-FONG SYNDROME 		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
Entrez Id: 9894
Gene Symbol: TELO2
TELO2
CUI: C4310778
Disease:
YOU-HOOVER-FONG SYNDROME 		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
Entrez Id: 9894
Gene Symbol: TELO2
TELO2
CUI: C4310778
Disease:
YOU-HOOVER-FONG SYNDROME 		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
Entrez Id: 9894
Gene Symbol: TELO2
TELO2
CUI: C4310778
Disease:
YOU-HOOVER-FONG SYNDROME 		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
Entrez Id: 9894
Gene Symbol: TELO2
TELO2
CUI: C4310778
Disease:
YOU-HOOVER-FONG SYNDROME 		T 0.800 GeneticVariation CLINVAR
dbSNP: rs202020308
rs202020308
Entrez Id: 9894
Gene Symbol: TELO2
TELO2
CUI: C4310778
Disease:
YOU-HOOVER-FONG SYNDROME 		T 0.800 CausalMutation CLINVAR
dbSNP: rs369656775
rs369656775
Entrez Id: 9894
Gene Symbol: TELO2
TELO2
CUI: C4310778
Disease:
YOU-HOOVER-FONG SYNDROME 		T 0.800 CausalMutation CLINVAR
dbSNP: rs371675497
rs371675497
Entrez Id: 9894
Gene Symbol: TELO2
TELO2
CUI: C4310778
Disease:
YOU-HOOVER-FONG SYNDROME 		A 0.800 CausalMutation CLINVAR
dbSNP: rs754162070
rs754162070
Entrez Id: 9894
Gene Symbol: TELO2
TELO2
CUI: C4310778
Disease:
YOU-HOOVER-FONG SYNDROME 		A 0.800 CausalMutation CLINVAR
dbSNP: rs878853271
rs878853271
Entrez Id: 9894
Gene Symbol: TELO2
TELO2
CUI: C4310778
Disease:
YOU-HOOVER-FONG SYNDROME 		T 0.800 CausalMutation CLINVAR
dbSNP: rs2745106
rs2745106
Entrez Id: 9894
Gene Symbol: TELO2
TELO2
CUI: C0003873
Disease:
Rheumatoid Arthritis 		G 0.700 GeneticVariation GWASCAT Studying the effects of haplotype partitioning methods on the RA-associated genomic results from the North American Rheumatoid Arthritis Consortium (NARAC) dataset. 30891314 2019
dbSNP: rs142217951
rs142217951
Entrez Id: 9894
Gene Symbol: TELO2
TELO2
CUI: C4310778
Disease:
YOU-HOOVER-FONG SYNDROME 		G 0.700 GeneticVariation CLINVAR