Variant (rsID / SNP)

rs370571609

rs370571609 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DIABLO. Location: chromosome 12, position 122,702,807. Clinical significance in the table: Conflicting interpretations of pathogenicity.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

DIABLOConflicting interpretations

Clinical significance (as recorded): Conflicting interpretations of pathogenicity
Variant type: single nucleotide variant
Chromosome / position: 12:122702807
Cytoband: 12q24.31
HGVS: NM_001371333.1(DIABLO):c.315+6T>A
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.