Variant (rsID / SNP)
rs61739186
rs61739186 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KIR3DX1. Location: chromosome 19, position 55,045,042. The table records no clinical significance for this variant.
Reference-table entries
KIR3DX1Not classified
- Variant type
- non_coding_transcript_exon_variant
- Chromosome / position
- 19:55045042
- HGVS
- NR_026716.2,n.268G>A
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.