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Variant (rsID / SNP)

rs1128552

SCLY

rs1128552 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SCLY. Location: chromosome 2, position 238,999,883. The table records no clinical significance for this variant.

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Reference-table entries

SCLYNot classified
Variant type
synonymous_variant
Chromosome / position
2:238999883
HGVS
NM_016510.7,c.909T>C,p.Ala303Ala
Allele change
Silent

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.