Variant (rsID / SNP)
rs1841957
rs1841957 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KLRC4. Location: chromosome 12, position 10,562,025. The table records no clinical significance for this variant.
Reference-table entries
KLRC4Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 12:10562025
- HGVS
- NM_013431.2,c.150G>A,p.Ser50Ser
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.