Variant (rsID / SNP)

rs897738

rs897738 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ADGRE1. Location: chromosome 19, position 6,901,891. The table records no clinical significance for this variant.

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Reference-table entries

ADGRE1Not classified

Variant type: missense_variant
Chromosome / position: 19:6901891
HGVS: NM_001974.5,c.520G>A,p.Asp174Asn
Allele change: Silent

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.