Variant (rsID / SNP)

rs55971546

rs55971546 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC10A2. Location: chromosome 13, position 103,718,308. Clinical significance in the table: Benign.

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Reference-table entries

SLC10A2Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 13:103718308
Cytoband: 13q33.1
HGVS: NM_000452.3(SLC10A2):c.292G>A (p.Val98Ile)
Allele change: Missense_V98I

Public references

dbSNP
ClinVar
Ensembl
gnomAD

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