Variant (rsID / SNP)
rs1056185
rs1056185 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZNF83, ZNF701. Location: chromosome 19, position 53,117,531. The table records no clinical significance for this variant.
Reference-table entries
ZNF83Not classified
- Variant type
- missense_variant
- Chromosome / position
- 19:53117531
- HGVS
- NM_001105549.2,c.287G>A,p.Ser96Asn
- Allele change
- Missense_S96N
Associated conditions / phenotypes
Missense_S96N|Missense_S96N|Missense_S96N|Missense_S96N|Missense_S96N|Missense_S96N|Missense_S96N|Missense_S96N|Missense_S96N|Missense_S96N|Missense_S96N|Missense_S96N
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.