Variant (rsID / SNP)

rs11968529

rs11968529 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MOCS1. Location: chromosome 6, position 39,873,755. Clinical significance in the table: Benign.

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Reference-table entries

MOCS1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 6:39873755
Cytoband: 6p21.2
HGVS: NM_001358530.2(MOCS1):c.*378G>A
Allele change: Silent

Associated conditions / phenotypes

Sulfite oxidase deficiency due to molybdenum cofactor deficiency type A

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.