Variant (rsID / SNP)

rs35536751

rs35536751 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to POT1. Location: chromosome 7, position 124,481,185. Clinical significance in the table: Benign.

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Reference-table entries

POT1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 7:124481185
Cytoband: 7q31.33
HGVS: NM_015450.3(POT1):c.1211G>T (p.Gly404Val)
Allele change: Silent

Associated conditions / phenotypes

Melanoma, cutaneous malignant, susceptibility to, 10|Hereditary cancer-predisposing syndrome

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.