Variant (rsID / SNP)
rs14309
RNASEK-C17ORF49RNASEK-C17orf49C17orf49
rs14309 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RNASEK-C17ORF49, RNASEK-C17orf49, C17orf49. Location: chromosome 17, position 6,919,093. The table records no clinical significance for this variant.
Reference-table entries
- Variant type
- splice_region_variant&non_coding_transcript_exon_variant
- Chromosome / position
- 17:6919093
- HGVS
- NR_037717.1,n.1248T>C
- Allele change
- Silent
Associated conditions / phenotypes
Peripheral Artery Disease|Type 2 Diabetes Mellitus|Microvascular Complications of Diabetes 6|Microvascular Complications of Diabetes 4|Microvascular Complications of Diabetes 3|Microvascular Complications of Diabetes 7|Chronic Kidney Disease|Lipid Metabolism Disorder
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.