Variant (rsID / SNP)

rs9973235

rs9973235 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PLIN3. Location: chromosome 19, position 4,847,713. The table records no clinical significance for this variant.

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Reference-table entries

PLIN3Not classified

Variant type: missense_variant
Chromosome / position: 19:4847713
HGVS: NM_005817.5,c.824T>C,p.Val275Ala
Allele change: Missense_V275A

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.