Variant (rsID / SNP)

rs145890655

rs145890655 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ASCC3. Location: chromosome 6, position 101,215,020. Clinical significance in the table: Uncertain significance.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

ASCC3Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 6:101215020
Cytoband: 6q16.3
HGVS: NM_006828.4(ASCC3):c.1596+1G>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.