Variant (rsID / SNP)

rs11790683

rs11790683 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to UNC13B. Location: chromosome 9, position 35,302,059. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

UNC13BNot classified

Variant type: synonymous_variant
Chromosome / position: 9:35302059
HGVS: NM_001371189.2,c.2658T>C,p.Pro886Pro
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.