Variant (rsID / SNP)
rs11070136
rs11070136 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DZIP1. Location: chromosome 13, position 96,239,805. The table records no clinical significance for this variant.
Reference-table entries
DZIP1Not classified
- Variant type
- missense_variant
- Chromosome / position
- 13:96239805
- HGVS
- NM_198968.4,c.2206C>T,p.Pro736Ser
- Allele change
- Missense_P717S
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.