Variant (rsID / SNP)

rs34264048

rs34264048 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SARS2, MRPS12. Location: chromosome 19, position 39,421,274. Clinical significance in the table: Benign.

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Reference-table entries

SARS2Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 19:39421274
Cytoband: 19q13.2
HGVS: NM_017827.4(SARS2):c.103A>G (p.Thr35Ala)
Allele change: Missense_T35A

Associated conditions / phenotypes

Hyperuricemia, pulmonary hypertension, renal failure, alkalosis syndrome

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.