Variant (rsID / SNP)
rs771205
rs771205 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MINDY1. Location: chromosome 1, position 150,975,108. The table records no clinical significance for this variant.
Reference-table entries
MINDY1Not classified
- Variant type
- 5_prime_UTR_variant
- Chromosome / position
- 1:150975108
- HGVS
- NM_001376664.1,c.-15A>G
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.