Variant (rsID / SNP)

rs7066252

rs7066252 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DRP2. The table records no clinical significance for this variant.

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Reference-table entries

DRP2Not classified

Variant type: missense_variant
HGVS: NM_001939.3,c.202G>C,p.Val68Leu
Allele change: 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.