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Variant (rsID / SNP)

rs145199539

FAM161A

rs145199539 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FAM161A. Location: chromosome 2, position 62,069,482. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

FAM161AConflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
2:62069482
Cytoband
2p15
HGVS
NM_001201543.2(FAM161A):c.197C>T (p.Thr66Ile)
Allele change
Silent

Associated conditions / phenotypes

Retinitis pigmentosa|Retinitis pigmentosa 28

Public references

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