Variant (rsID / SNP)

rs739231

rs739231 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PNPLA5. Location: chromosome 22, position 44,282,276. The table records no clinical significance for this variant.

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Reference-table entries

PNPLA5Not classified

Variant type: missense_variant
Chromosome / position: 22:44282276
HGVS: NM_138814.4,c.856T>C,p.Trp286Arg
Allele change: Missense_W286R

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.