Variant (rsID / SNP)

rs2253869

rs2253869 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZNF316. Location: chromosome 7, position 6,683,454. The table records no clinical significance for this variant.

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Reference-table entries

ZNF316Not classified

Variant type: missense_variant&splice_region_variant
Chromosome / position: 7:6683454
HGVS: NM_001278559.2,c.467A>G,p.Glu156Gly
Allele change: Missense_E156G

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.