Variant (rsID / SNP)

rs200989342

rs200989342 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RINT1. Location: chromosome 7, position 105,190,613. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

RINT1Conflicting interpretations

Clinical significance (as recorded): Conflicting interpretations of pathogenicity
Variant type: single nucleotide variant
Chromosome / position: 7:105190613
Cytoband: 7q22.3
HGVS: NM_021930.6(RINT1):c.1107+1G>T
Allele change: Silent

Associated conditions / phenotypes

Thyroid cancer, nonmedullary, 1

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.