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Variant (rsID / SNP)

rs45552433

SULT6B1

rs45552433 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SULT6B1. Location: chromosome 2, position 37,415,603. The table records no clinical significance for this variant.

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Reference-table entries

SULT6B1Not classified
Variant type
missense_variant
Chromosome / position
2:37415603
HGVS
NM_001367551.1,c.181G>A,p.Ala61Thr
Allele change
Missense_A23T

Public references

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