Variant (rsID / SNP)

rs11577368

rs11577368 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PARS2. Location: chromosome 1, position 55,224,751. Clinical significance in the table: Benign.

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Reference-table entries

PARS2Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 1:55224751
Cytoband: 1p32.3
HGVS: NM_152268.4(PARS2):c.84G>T (p.Arg28Ser)
Allele change: Missense_R28S

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.