Variant (rsID / SNP)

rs62317770

rs62317770 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LARP7. Location: chromosome 4, position 113,568,544. 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: 4:113568544
Cytoband: 4q25
HGVS: NM_016648.4(LARP7):c.836G>A (p.Arg279Gln)
Allele change: Missense_R279Q

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.