Variant (rsID / SNP)
rs6949654
rs6949654 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GSAP. Location: chromosome 7, position 77,035,392. The table records no clinical significance for this variant.
Reference-table entries
GSAPNot classified
- Variant type
- missense_variant
- Chromosome / position
- 7:77035392
- HGVS
- NM_001350896.2,c.140A>G,p.His47Arg
- Allele change
- Missense_H47R
Associated conditions / phenotypes
Silent|Missense_H47R|Missense_H47R
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.