Variant (rsID / SNP)

rs7625806

rs7625806 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DLEC1. Location: chromosome 3, position 38,080,952. The table records no clinical significance for this variant.

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Reference-table entries

DLEC1Not classified

Variant type: missense_variant
Chromosome / position: 3:38080952
HGVS: NM_007337.4,c.236T>G,p.Leu79Arg
Allele change: Missense_L79R

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.