Variant (rsID / SNP)

rs56202530

rs56202530 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PALM3. Location: chromosome 19, position 14,165,278. The table records no clinical significance for this variant.

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Reference-table entries

PALM3Not classified

Variant type: synonymous_variant
Chromosome / position: 19:14165278
HGVS: NM_001145028.2,c.1206C>T,p.Gly402Gly
Allele change: Synonymous_G387G

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.