Variant (rsID / SNP)
rs7494786
rs7494786 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HERC2. Location: chromosome 15, position 28,414,665. The table records no clinical significance for this variant.
Reference-table entries
HERC2Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 15:28414665
- HGVS
- NM_004667.6,c.10194A>G,p.Ser3398Ser
- Allele change
- Synonymous_S3398S
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.