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Variant (rsID / SNP)

rs3748930

CHST10

rs3748930 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CHST10. Location: chromosome 2, position 101,010,082. The table records no clinical significance for this variant.

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Reference-table entries

CHST10Not classified
Variant type
synonymous_variant
Chromosome / position
2:101010082
HGVS
NM_004854.5,c.696C>G,p.Thr232Thr
Allele change
Synonymous_T232T

Public references

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