Variant (rsID / SNP)

rs377289876

rs377289876 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to JUN. Location: chromosome 1, position 59,248,085. The table records no clinical significance for this variant.

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Reference-table entries

JUNNot classified

Variant type: single nucleotide variant
Chromosome / position: 1:59248085
Cytoband: 1p32.1
HGVS: NM_002228.4(JUN):c.658C>G (p.Pro220Ala)
Allele change: Missense_P220A

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.