Variant (rsID / SNP)

rs183615774

rs183615774 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FAM161A. Location: chromosome 2, position 62,067,223. Clinical significance in the table: Uncertain significance.

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Reference-table entries

FAM161AUncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 2:62067223
Cytoband: 2p15
HGVS: NM_001201543.2(FAM161A):c.916C>T (p.Arg306Trp)
Allele change: Silent

Associated conditions / phenotypes

Retinitis pigmentosa|Retinitis pigmentosa 28

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.