Variant (rsID / SNP)

rs34745784

rs34745784 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ARV1. Location: chromosome 1, position 231,114,945. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

ARV1Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 1:231114945
Cytoband: 1q42.2
HGVS: NM_022786.3(ARV1):c.94T>C (p.Tyr32His)
Allele change: Missense_Y32H

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.