Variant (rsID / SNP)

rs2228539

rs2228539 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ADGRE1. Location: chromosome 19, position 6,926,378. The table records no clinical significance for this variant.

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Reference-table entries

ADGRE1Not classified

Variant type: missense_variant&splice_region_variant
Chromosome / position: 19:6926378
HGVS: NM_001974.5,c.1988T>C,p.Met663Thr
Allele change: Missense_M522T

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.