Variant (rsID / SNP)
rs12625565
rs12625565 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LPIN3. Location: chromosome 20, position 39,986,085. The table records no clinical significance for this variant.
Reference-table entries
LPIN3Not classified
- Variant type
- missense_variant&splice_region_variant
- Chromosome / position
- 20:39986085
- HGVS
- NM_001301860.2,c.2040A>C,p.Gln680His
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.