Variant (rsID / SNP)
rs1057463
C8ORF44-SGK3C8orf44C8orf44-SGK3
rs1057463 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to C8ORF44-SGK3, C8orf44, C8orf44-SGK3. Location: chromosome 8, position 67,592,152. The table records no clinical significance for this variant.
Reference-table entries
C8ORF44-SGK3Not classified
- Variant type
- 5_prime_UTR_variant
- Chromosome / position
- 8:67592152
- HGVS
- NM_001204173.2,c.-285T>C
- Allele change
- Missense_F148S
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.