Variant (rsID / SNP)
rs2642992
rs2642992 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZNF695. Location: chromosome 1, position 247,151,557. The table records no clinical significance for this variant.
Reference-table entries
ZNF695Not classified
- Variant type
- missense_variant&splice_region_variant
- Chromosome / position
- 1:247151557
- HGVS
- NM_020394.5,c.260T>C,p.Val87Ala
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.