Variant (rsID / SNP)

rs141934766

rs141934766 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SNAP29. Location: chromosome 22, position 21,241,976. Clinical significance in the table: Uncertain significance.

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Reference-table entries

SNAP29Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 22:21241976
Cytoband: 22q11.21
HGVS: NM_004782.4(SNAP29):c.629C>T (p.Ser210Phe)
Allele change: Missense_S210F

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.