Variant (rsID / SNP)

rs11686212

rs11686212 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TRAPPC12. Location: chromosome 2, position 3,392,295. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

TRAPPC12Not classified

Variant type: missense_variant
Chromosome / position: 2:3392295
HGVS: NM_001321102.2,c.901A>G,p.Ser301Gly
Allele change: Missense_S301G

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.