Variant (rsID / SNP)
rs910397
rs910397 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PXMP4. Location: chromosome 20, position 32,295,541. The table records no clinical significance for this variant.
Reference-table entries
PXMP4Not classified
- Variant type
- missense_variant
- Chromosome / position
- 20:32295541
- HGVS
- NM_007238.5,c.610G>A,p.Val204Ile
- Allele change
- Missense_V204I
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.