Variant (rsID / SNP)

rs165815

rs165815 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ARVCF. Location: chromosome 22, position 19,959,473. The table records no clinical significance for this variant.

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Reference-table entries

ARVCFNot classified

Variant type: missense_variant
Chromosome / position: 22:19959473
HGVS: NM_001670.3,c.2717G>A,p.Arg906Gln
Allele change: Missense_R906Q

Associated conditions / phenotypes

Schizophrenia|Velocardiofacial Syndrome|Tremor|Rem Sleep Behavior Disorder|Pure Autonomic Failure

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.