Variant (rsID / SNP)
rs9972951
rs9972951 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ARSG. Location: chromosome 17, position 66,391,276. The table records no clinical significance for this variant.
Reference-table entries
ARSGNot classified
- Variant type
- missense_variant
- Chromosome / position
- 17:66391276
- HGVS
- NM_001267727.2,c.1154G>A,p.Arg385His
- Allele change
- Missense_R384H
Associated conditions / phenotypes
Missense_R385H|Missense_R369H|Missense_R385H|Missense_R384H|Missense_R385H|Missense_R385H|Missense_R385H|Missense_R385H
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.