Variant (rsID / SNP)
rs80127039
rs80127039 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NRG1. Location: chromosome 8, position 32,621,630. The table records no clinical significance for this variant.
Reference-table entries
NRG1Not classified
- Variant type
- missense_variant
- Chromosome / position
- 8:32621630
- HGVS
- NM_001322205.2,c.1813C>T,p.Arg605Trp
- Allele change
- Missense_R550W
Associated conditions / phenotypes
Missense_P500L|Missense_P483L|Missense_R287W|Missense_P517L|Missense_R287W|Missense_R605W|Silent|Missense_R388W
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.