Variant (rsID / SNP)
rs11832661
rs11832661 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to R3HDM2. Location: chromosome 12, position 57,704,109. The table records no clinical significance for this variant.
Reference-table entries
R3HDM2Not classified
- Variant type
- missense_variant
- Chromosome / position
- 12:57704109
- HGVS
- NM_001351204.2,c.103A>G,p.Thr35Ala
- Allele change
- Missense_T35A
Associated conditions / phenotypes
Missense_T35A|Missense_T35A|Missense_T35A|Missense_T35A|Missense_T35A|Missense_T35A|Missense_T35A|Missense_T35A|Missense_T35A|Missense_T35A|Missense_T35A|Missense_T35A|Missense_T35A
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.