Variant (rsID / SNP)

rs79383654

rs79383654 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LARP7. Location: chromosome 4, position 113,565,835. Clinical significance in the table: Benign.

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Reference-table entries

LARP7Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 4:113565835
Cytoband: 4q25
HGVS: NM_016648.4(LARP7):c.10G>A (p.Glu4Lys)
Allele change: Missense_E4K

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.