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Variant (rsID / SNP)

rs112657170

SLC10A2

rs112657170 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC10A2. Location: chromosome 13, position 103,718,406. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

SLC10A2Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
13:103718406
Cytoband
13q33.1
HGVS
NM_000452.3(SLC10A2):c.194C>T (p.Pro65Leu)
Allele change
Missense_P65L

Public references

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