Variant (rsID / SNP)

rs118056333

rs118056333 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SULF1. Location: chromosome 8, position 70,515,476. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

SULF1Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 8:70515476
Cytoband: 8q13.3
HGVS: NM_001128205.2(SULF1):c.1111A>G (p.Ile371Val)
Allele change: Missense_I371V

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.