Variant (rsID / SNP)
rs75117355
rs75117355 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PLXDC1. Location: chromosome 17, position 37,224,211. The table records no clinical significance for this variant.
Reference-table entries
PLXDC1Not classified
- Variant type
- missense_variant&splice_region_variant
- Chromosome / position
- 17:37224211
- HGVS
- NM_020405.5,c.1385G>A,p.Arg462His
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.