Variant (rsID / SNP)

rs307772

rs307772 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DENND3. Location: chromosome 8, position 142,146,708. The table records no clinical significance for this variant.

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Reference-table entries

DENND3Not classified

Variant type: start_lost
Chromosome / position: 8:142146708
HGVS: NM_014957.5,c.2T>C,p.Met1?
Allele change: Missense_M68T

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.