Variant (rsID / SNP)

rs112050262

rs112050262 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SULT1C3. Location: chromosome 2, position 108,863,758. Clinical significance in the table: Benign.

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Reference-table entries

SULT1C3Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 2:108863758
Cytoband: 2q12.3
HGVS: NM_001320878.2(SULT1C3):c.108G>A (p.Trp36Ter)
Allele change: Nonsense_W36X

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.