Variant (rsID / SNP)

rs530978

rs530978 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PRUNE2. Location: chromosome 9, position 79,324,179. The table records no clinical significance for this variant.

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Reference-table entries

PRUNE2Not classified

Variant type: missense_variant
Chromosome / position: 9:79324179
HGVS: NM_015225.3,c.3011C>T,p.Thr1004Met
Allele change: Missense_T1004M

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.