Variant (rsID / SNP)
rs2231940
rs2231940 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DMAC2. Location: chromosome 19, position 41,944,237. The table records no clinical significance for this variant.
Reference-table entries
DMAC2Not classified
- Variant type
- missense_variant
- Chromosome / position
- 19:41944237
- HGVS
- NM_001167867.2,c.119A>G,p.Asn40Ser
- Allele change
- Silent
Associated conditions / phenotypes
Missense_N34S|Missense_N40S|Missense_N34S|Missense_N34S|Silent|Missense_N34S|Silent|Missense_N40S|Missense_N34S
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.