Variant (rsID / SNP)
rs3731958
rs3731958 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GTDC1. Location: chromosome 2, position 144,899,559. The table records no clinical significance for this variant.
Reference-table entries
GTDC1Not classified
- Variant type
- missense_variant
- Chromosome / position
- 2:144899559
- HGVS
- NM_001376306.2,c.411G>T,p.Met137Ile
- Allele change
- Missense_M8I
Associated conditions / phenotypes
Missense_M137I|Missense_M137I|Silent|Missense_M105I|Silent|Missense_M137I|Missense_M137I|Missense_M137I|Missense_M137I|Missense_M137I|Missense_M8I|Missense_M137I|Missense_M137I|Missense_M137I
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.