Variant (rsID / SNP)
rs1122955
rs1122955 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZNF132. Location: chromosome 19, position 58,946,203. The table records no clinical significance for this variant.
Reference-table entries
ZNF132Not classified
- Variant type
- missense_variant
- Chromosome / position
- 19:58946203
- HGVS
- NM_003433.4,c.608G>A,p.Gly203Asp
- Allele change
- Missense_G203D
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.