Variant (rsID / SNP)

rs13346368

rs13346368 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to BICRA. Location: chromosome 19, position 48,198,675. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

BICRANot classified

Variant type: missense_variant
Chromosome / position: 19:48198675
HGVS: NM_001394372.1,c.3130A>G,p.Thr1044Ala
Allele change: Missense_T1044A

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.