Variant (rsID / SNP)
rs111417655
rs111417655 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC27A4. Location: chromosome 9, position 131,115,368. Clinical significance in the table: not_provided.
Reference-table entries
SLC27A4Other
- Clinical significance (as recorded)
- not_provided
- Variant type
- missense_variant
- Chromosome / position
- 9:131115368
- HGVS
- NM_005094.4,c.1052A>G,p.Asn351Ser
- Allele change
- Missense_N351S
Associated conditions / phenotypes
Ichthyosis Prematurity Syndrome
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.