Variant (rsID / SNP)
rs2245623
rs2245623 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RHBG. Location: chromosome 1, position 156,347,131. The table records no clinical significance for this variant.
Reference-table entries
RHBGNot classified
- Variant type
- missense_variant
- Chromosome / position
- 1:156347131
- HGVS
- NM_020407.5,c.227G>A,p.Gly76Asp
- Allele change
- Silent
Associated conditions / phenotypes
Missense_G76D|Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.