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Variant (rsID / SNP)

rs11083907

SULT2A1

rs11083907 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SULT2A1. Location: chromosome 19, position 48,389,425. The table records no clinical significance for this variant.

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Reference-table entries

SULT2A1Not classified
Variant type
synonymous_variant
Chromosome / position
19:48389425
HGVS
NM_003167.4,c.90T>C,p.Phe30Phe
Allele change
Synonymous_F30F

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.