Variant (rsID / SNP)

rs78163218

rs78163218 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RASSF3. Location: chromosome 12, position 65,068,169. The table records no clinical significance for this variant.

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Reference-table entries

RASSF3Not classified

Variant type: intron_variant
Chromosome / position: 12:65068169
HGVS: NM_178169.4,c.112-10398G>A
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.