Variant (rsID / SNP)

rs2229722

rs2229722 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to VIPR1. Location: chromosome 3, position 42,568,929. The table records no clinical significance for this variant.

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Reference-table entries

VIPR1Not classified

Variant type: synonymous_variant
Chromosome / position: 3:42568929
HGVS: NM_004624.4,c.444T>C,p.Ile148Ile
Allele change: Synonymous_I107I

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.