Variant (rsID / SNP)
rs15350
rs15350 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NFATC1. Location: chromosome 18, position 77,211,764. The table records no clinical significance for this variant.
Reference-table entries
NFATC1Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 18:77211764
- HGVS
- NM_001278669.2,c.1851T>C,p.Ser617Ser
- Allele change
- Synonymous_S145S
Associated conditions / phenotypes
Synonymous_S604S|Synonymous_S604S|Synonymous_S604S|Synonymous_S145S|Synonymous_S604S
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.