Variant (rsID / SNP)
rs2617170
rs2617170 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KLRC4. Location: chromosome 12, position 10,560,957. The table records no clinical significance for this variant.
Reference-table entries
KLRC4Not classified
- Variant type
- missense_variant
- Chromosome / position
- 12:10560957
- HGVS
- NM_013431.2,c.311A>G,p.Asn104Ser
- Allele change
- Silent
Associated conditions / phenotypes
Autoimmune Disease|Hepatitis B|Vasculitis
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.