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Variant (rsID / SNP)

rs202066007

ADGRV1

rs202066007 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ADGRV1. Location: chromosome 5, position 90,059,208. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

ADGRV1Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
5:90059208
Cytoband
5q14.3
HGVS
NM_032119.4(ADGRV1):c.12207C>T (p.Thr4069=)
Allele change
Synonymous_T4069T

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.