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Variant (rsID / SNP)

rs10841611

SLCO1C1

rs10841611 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLCO1C1. Location: chromosome 12, position 20,903,757. The table records no clinical significance for this variant.

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Reference-table entries

SLCO1C1Not classified
Variant type
synonymous_variant
Chromosome / position
12:20903757
HGVS
NM_001145946.2,c.1947T>C,p.His649His
Allele change
Synonymous_H649H

Public references

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