Variant (rsID / SNP)

rs114211101

rs114211101 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TG. Location: chromosome 8, position 134,125,846. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

TGConflicting interpretations

Clinical significance (as recorded): Conflicting interpretations of pathogenicity
Variant type: single nucleotide variant
Chromosome / position: 8:134125846
Cytoband: 8q24.22
HGVS: NM_003235.5(TG):c.7753C>T (p.Arg2585Trp)
Allele change: Missense_R2585W

Associated conditions / phenotypes

Iodotyrosyl coupling defect

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.