Variant (rsID / SNP)
rs77387993
rs77387993 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MUC22. Location: chromosome 6, position 30,994,730. The table records no clinical significance for this variant.
Reference-table entries
MUC22Not classified
- Variant type
- missense_variant
- Chromosome / position
- 6:30994730
- HGVS
- NM_001318484.1,c.1531G>A,p.Ala511Thr
- Allele change
- Missense_A508T
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.