Variant (rsID / SNP)

rs121917877

rs121917877 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SSTR5. Location: chromosome 16, position 1,129,586. Clinical significance in the table: Benign.

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Reference-table entries

SSTR5Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 16:1129586
Cytoband: 16p13.3
HGVS: NM_001172560.3(SSTR5):c.718C>T (p.Arg240Trp)
Allele change: Missense_R240W

Associated conditions / phenotypes

Somatostatin analog, resistance to

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.