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Variant (rsID / SNP)

rs35001260

DENND1C

rs35001260 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DENND1C. Location: chromosome 19, position 6,468,907. The table records no clinical significance for this variant.

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Reference-table entries

DENND1CNot classified
Variant type
missense_variant
Chromosome / position
19:6468907
HGVS
NM_024898.4,c.1465C>T,p.Arg489Cys
Allele change
Missense_R445C

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.