Variant (rsID / SNP)

rs111753827

rs111753827 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ADGRV1. Location: chromosome 5, position 89,968,474. Clinical significance in the table: Benign.

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Reference-table entries

ADGRV1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 5:89968474
Cytoband: 5q14.3
HGVS: NM_032119.4(ADGRV1):c.4864T>C (p.Tyr1622His)
Allele change: Missense_Y1622H

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.