Variant (rsID / SNP)

rs330877

rs330877 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ADGRE1. Location: chromosome 19, position 6,896,483. The table records no clinical significance for this variant.

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Reference-table entries

ADGRE1Not classified

Variant type: missense_variant
Chromosome / position: 19:6896483
HGVS: NM_001974.5,c.169G>A,p.Ala57Thr
Allele change: Missense_A57T

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.