Variant (rsID / SNP)

rs3803892

rs3803892 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to BRME1. Location: chromosome 19, position 14,000,170. The table records no clinical significance for this variant.

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Reference-table entries

BRME1Not classified

Variant type: missense_variant
Chromosome / position: 19:14000170
HGVS: NM_001345843.2,c.1499A>G,p.Gln500Arg
Allele change: Missense_Q382R

Associated conditions / phenotypes

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.