Variant (rsID / SNP)

rs2228497

rs2228497 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SSTR1. Location: chromosome 14, position 38,679,473. The table records no clinical significance for this variant.

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Reference-table entries

SSTR1Not classified

Variant type: synonymous_variant
Chromosome / position: 14:38679473
HGVS: NM_001049.3,c.879C>T,p.Val293Val
Allele change: Synonymous_V293V

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.