Variant (rsID / SNP)

rs7014062

rs7014062 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DENND3. Location: chromosome 8, position 142,202,884. The table records no clinical significance for this variant.

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Reference-table entries

DENND3Not classified

Variant type: missense_variant
Chromosome / position: 8:142202884
HGVS: NM_001362798.2,c.3758T>C,p.Val1253Ala
Allele change: Missense_V1253A

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.