Variant (rsID / SNP)

rs1983609

rs1983609 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PARVB. Location: chromosome 22, position 44,489,868. The table records no clinical significance for this variant.

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Reference-table entries

PARVBNot classified

Variant type: missense_variant
Chromosome / position: 22:44489868
HGVS: NM_001003828.3,c.272T>C,p.Val91Ala
Allele change: Missense_V91A

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.