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Variant (rsID / SNP)

rs2219078

SULT1C3

rs2219078 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SULT1C3. Location: chromosome 2, position 108,875,198. The table records no clinical significance for this variant.

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Reference-table entries

SULT1C3Not classified
Variant type
missense_variant
Chromosome / position
2:108875198
HGVS
NM_001008743.3,c.535G>A,p.Gly179Arg
Allele change
Missense_G179R

Public references

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