Variant (rsID / SNP)
rs1975349
rs1975349 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZNF788P. Location: chromosome 19, position 12,222,861. The table records no clinical significance for this variant.
Reference-table entries
ZNF788PNot classified
- Variant type
- non_coding_transcript_exon_variant
- Chromosome / position
- 19:12222861
- HGVS
- NR_171040.1,n.1223T>C
- Allele change
- Missense_C167R
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.