Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1553915580
rs1553915580
TT 0.700 CausalMutation CLINVAR Novel variants in Nordic patients referred for genetic testing of telomere-related disorders. 29483670

2018

dbSNP: rs1553915612
rs1553915612
T 0.700 CausalMutation CLINVAR Novel variants in Nordic patients referred for genetic testing of telomere-related disorders. 29483670

2018

dbSNP: rs1553915617
rs1553915617
A 0.700 CausalMutation CLINVAR Novel variants in Nordic patients referred for genetic testing of telomere-related disorders. 29483670

2018

dbSNP: rs1553915621
rs1553915621
GGCGCCT 0.700 CausalMutation CLINVAR Novel variants in Nordic patients referred for genetic testing of telomere-related disorders. 29483670

2018

dbSNP: rs199422265
rs199422265
C 0.700 CausalMutation CLINVAR

dbSNP: rs199422268
rs199422268
T 0.700 CausalMutation CLINVAR

dbSNP: rs199422270
rs199422270
A 0.700 CausalMutation CLINVAR

dbSNP: rs199422272
rs199422272
A 0.700 CausalMutation CLINVAR

dbSNP: rs199422277
rs199422277
C 0.700 CausalMutation CLINVAR