Variant (rsID / SNP)

rs1862514

rs1862514 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to STXBP2, PCP2. Location: chromosome 19, position 7,698,320. Clinical significance in the table: Benign.

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Reference-table entries

STXBP2Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 19:7698320
Cytoband: 19p13.2
HGVS: NM_174895.3(PCP2):c.24G>A (p.Thr8_Glu9=)
Allele change: Synonymous_T8T

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.