Variant (rsID / SNP)
rs3765121
rs3765121 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KCNIP4. Location: chromosome 4, position 20,852,166. The table records no clinical significance for this variant.
Reference-table entries
KCNIP4Not classified
- Variant type
- splice_region_variant&synonymous_variant
- Chromosome / position
- 4:20852166
- HGVS
- NM_025221.6,c.288T>C,p.Asn96Asn
- Allele change
- Synonymous_N34N
Associated conditions / phenotypes
Synonymous_N34N|Synonymous_N79N
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.