Variant (rsID / SNP)

rs200106260

rs200106260 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ADGRV1. Location: chromosome 5, position 90,041,590. Clinical significance in the table: Likely benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

ADGRV1Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 5:90041590
Cytoband: 5q14.3
HGVS: NM_032119.4(ADGRV1):c.10952A>G (p.Tyr3651Cys)
Allele change: Missense_Y3651C

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.