Variant (rsID / SNP)

rs4829830

rs4829830 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ADGRG4. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

ADGRG4Not classified

Variant type: missense_variant
HGVS: NM_153834.4,c.3638C>A,p.Thr1213Asn
Allele change: Missense_T1213N

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.