Variant (rsID / SNP)
rs3213690
rs3213690 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to AMZ2. Location: chromosome 17, position 66,246,416. The table records no clinical significance for this variant.
Reference-table entries
AMZ2Not classified
- Variant type
- missense_variant
- Chromosome / position
- 17:66246416
- HGVS
- NM_001033569.2,c.88A>G,p.Asn30Asp
- Allele change
- Missense_N30D
Associated conditions / phenotypes
Missense_N30D|Missense_N30D|Silent|Missense_N30D|Missense_N30D|Silent|Missense_N30D|Missense_N30D|Missense_N30D|Missense_N30D|Missense_N30D|Missense_N30D|Missense_N30D|Silent|Missense_N30D|Missense_N30D|Silent|Missense_N30D
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.