rs199422230
A SNP in the IDS gene on chromosome X. Its most notable genotype is C;T: Carrier of a MPS II mutation; note X-linkage
- Gene
- IDS
- Location
- Chr X149,482,974 (GRCh38)
- Highest magnitude
- 3.0Important
- Tested on
- AncestryDNA
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
- C;TMost notableBadCarrier of a MPS II mutation; note X-linkage
- C;CGoodcommon in clinvar
SNPedia records rs199422230 on the minus strand: (A;G), (G;G). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Related
Other IDS SNPs
- rs104894861C;TCarrier of a MPS II mutation; note X-linkageImportant
- rs113993946C;TCarrier of a MPS II mutation; note X-linkageImportant
- rs113993949C;TCarrier of a MPS II mutation; note X-linkageImportant
- rs113993952A;TCarrier of a MPS II mutation; note X-linkageImportant
- rs113993955A;GCarrier of a MPS II mutation; note X-linkageImportant
- rs193302910C;TCarrier of a MPS II mutation; note X-linkageImportant
- rs193302911G;TCarrier of a MPS II mutation; note X-linkageImportant
- rs199422227A;GCarrier of a MPS II mutation; note X-linkageImportant
Notes
From SNPedia
Notes
C;T
Unaffected in absence of another mutation in the IDS gene.
Source and license
Adapted from rs199422230 on SNPedia, using a snapshot taken October 16, 2026. SNPedia content is shared under CC BY-NC-SA 3.0 US, and this page is shared under the same license.
SNPedia is a community-edited wiki. Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice. Magnitude is a community rating of how interesting a genotype is, not a risk score.