Variant (rsID / SNP)

rs188096

rs188096 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC10A2. Location: chromosome 13, position 103,705,044. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

SLC10A2Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 13:103705044
Cytoband: 13q33.1
HGVS: NM_000452.3(SLC10A2):c.511T>G (p.Ser171Ala)
Allele change: Missense_S171A

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.