Variant (rsID / SNP)
rs17772929
rs17772929 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC5A11. Location: chromosome 16, position 24,918,048. The table records no clinical significance for this variant.
Reference-table entries
SLC5A11Not classified
- Variant type
- missense_variant
- Chromosome / position
- 16:24918048
- HGVS
- NM_001258414.2,c.679C>T,p.Arg227Cys
- Allele change
- Silent
Associated conditions / phenotypes
Synonymous_I324I|Synonymous_I260I|Silent|Missense_R291C|Silent|Synonymous_I346I|Silent|Synonymous_I332I|Synonymous_I289I|Synonymous_I295I|Missense_R227C|Silent|Synonymous_I295I|Synonymous_I324I|Synonymous_I359I|Missense_R291C|Synonymous_I295I|Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.