Variant (rsID / SNP)

rs78686793

rs78686793 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SIPA1L3. Location: chromosome 19, position 38,643,539. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

SIPA1L3Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 19:38643539
Cytoband: 19q13.13
HGVS: NM_015073.3(SIPA1L3):c.3593C>T (p.Thr1198Met)
Allele change: Missense_T1198M

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.