Variant (rsID / SNP)

rs61736946

rs61736946 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HARS2. Location: chromosome 5, position 140,076,899. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

HARS2Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 5:140076899
Cytoband: 5q31.3
HGVS: NM_012208.4(HARS2):c.1105G>C (p.Gly369Arg)
Allele change: Missense_G369R

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.