Variant (rsID / SNP)
rs7017776
rs7017776 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CSGALNACT1. Location: chromosome 8, position 19,362,768. The table records no clinical significance for this variant.
Reference-table entries
CSGALNACT1Not classified
- Variant type
- missense_variant
- Chromosome / position
- 8:19362768
- HGVS
- NM_001130518.2,c.578G>A,p.Ser193Asn
- Allele change
- Missense_S193N
Associated conditions / phenotypes
Missense_S193N|Silent|Missense_S193N|Missense_S193N|Silent|Silent|Missense_S193N|Missense_S193N|Missense_S193N|Missense_S193N|Missense_S193N|Missense_S193N|Silent|Missense_S193N|Missense_S193N|Missense_S193N|Silent|Missense_S193N
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.