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Variant (rsID / SNP)

rs17036104

SULT1C2

rs17036104 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SULT1C2. Location: chromosome 2, position 108,922,036. The table records no clinical significance for this variant.

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Reference-table entries

SULT1C2Not classified
Variant type
missense_variant
Chromosome / position
2:108922036
HGVS
NM_176825.3,c.796T>G,p.Ser266Ala
Allele change
Missense_S266A

Public references

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