Variant (rsID / SNP)
rs41380347
rs41380347 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MCM6. Location: chromosome 2, position 136,608,651. Clinical significance in the table: association.
Reference-table entries
MCM6Association
- Clinical significance (as recorded)
- association
- Variant type
- single nucleotide variant
- Chromosome / position
- 2:136608651
- Cytoband
- 2q21.3
- HGVS
- NM_005915.6(MCM6):c.1917+321T>G
- Allele change
- Silent
Associated conditions / phenotypes
Lactase persistence
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.