Variant (rsID / SNP)

rs218966

rs218966 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PHF14. Location: chromosome 7, position 11,022,230. The table records no clinical significance for this variant.

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Reference-table entries

PHF14Not classified

Variant type: missense_variant
Chromosome / position: 7:11022230
HGVS: NM_001007157.2,c.344A>G,p.Lys115Arg
Allele change: Missense_R266G

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.