Variant (rsID / SNP)

rs73541957

rs73541957 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ASS1. Location: chromosome 9, position 133,329,682. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

ASS1Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 9:133329682
Cytoband: 9q34.11
HGVS: NM_054012.4(ASS1):c.106-10T>G
Allele change: Silent

Associated conditions / phenotypes

Citrullinemia type I|Citrullinemia

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.