Variant (rsID / SNP)
rs7041
rs7041 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GC. Location: chromosome 4, position 72,618,334. Clinical significance in the table: Benign.
Reference-table entries
GCBenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 4:72618334
- Cytoband
- 4q13.3
- HGVS
- NM_000583.4(GC):c.1296T>G (p.Asp432Glu)
- Allele change
- Missense_D432E
Associated conditions / phenotypes
GC1/GC2 POLYMORPHISM
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.