Variant (rsID / SNP)

rs376222680

rs376222680 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SYP. Clinical significance in the table: Uncertain significance.

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Reference-table entries

SYPUncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Cytoband: Xp11.23
HGVS: NM_003179.3(SYP):c.868G>T (p.Gly290Trp)
Allele change: Missense_G290W

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.