Variant (rsID / SNP)

rs117316516

rs117316516 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ANO6. Location: chromosome 12, position 45,797,209. Clinical significance in the table: Benign.

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Reference-table entries

ANO6Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 12:45797209
Cytoband: 12q12
HGVS: NM_001025356.3(ANO6):c.1783-13T>C
Allele change: Silent

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.