Variant (rsID / SNP)

rs13030

rs13030 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PSMC5. Location: chromosome 17, position 61,908,556. The table records no clinical significance for this variant.

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Reference-table entries

PSMC5Not classified

Variant type: synonymous_variant
Chromosome / position: 17:61908556
HGVS: NM_002805.6,c.840C>T,p.Leu280Leu
Allele change: Synonymous_L280L

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.