Variant (rsID / SNP)

rs3749427

rs3749427 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZNF695. Location: chromosome 1, position 247,150,740. The table records no clinical significance for this variant.

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Reference-table entries

ZNF695Not classified

Variant type: synonymous_variant
Chromosome / position: 1:247150740
HGVS: NM_020394.5,c.1077A>G,p.Lys359Lys
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.