Variant (rsID / SNP)

rs760482

rs760482 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DNAL4. Location: chromosome 22, position 39,178,701. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

DNAL4Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 22:39178701
Cytoband: 22q13.1
HGVS: NM_005740.3(DNAL4):c.36T>C (p.Asp12=)
Allele change: Synonymous_D12D

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.