Variant (rsID / SNP)

rs745599370

rs745599370 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SGCG. Location: chromosome 13, position 23,777,826. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

SGCGConflicting interpretations

Clinical significance (as recorded): Conflicting interpretations of pathogenicity
Variant type: single nucleotide variant
Chromosome / position: 13:23777826
Cytoband: 13q12.12
HGVS: NM_000231.3(SGCG):c.1-8C>T
Allele change: Silent

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.