rs1948948 UNGP1 - HNRNPA1L3
T allele associated with increased IDP dMRI TBSS ISOVF Sagittal stratum R (β=0.083). [GWAS Catalog]
What is rs1948948?
rs1948948 is a single-nucleotide polymorphism (SNP) in the UNGP1 - HNRNPA1L3 gene. Each person carries two copies, one from each parent, so a result is reported as a pair of letters such as TT. The table below describes what studies associate with each genotype; the association is statistical, across populations, and is not a diagnosis.
What does each rs1948948 genotype mean?
| Genotype | Association | What the evidence says | Confidence |
|---|---|---|---|
| TT | increased | T allele associated with increased IDP dMRI TBSS ISOVF Sagittal stratum R (β=0.083). [GWAS Catalog] | 75% |
| CC | typical | C allele associated with increased White matter hyperintensity volume (adjusted for hypertension) (β=0.037). [GWAS Catalog] | 65% |
Is rs1948948 on 23andMe and AncestryDNA chips?
Chip coverage is not recorded for this variant. Orviva reports it when a raw-data file contains it directly or via a well-correlated proxy SNP, and says so when it does not.
Sources
- PubMed 33293549
- GWAS Catalog
- GCST011950
Upload your 23andMe, AncestryDNA or WeGene raw file → · Ask G2: “What is my genotype at rs1948948 and what does it mean for me?”
Genetic associations describe risk across populations, not a diagnosis for any one person. Most variants shift risk modestly and act alongside lifestyle, environment and other genes. Consumer DNA chips do not read every position and can be wrong at any single one. For general education only; talk to a clinician or genetic counsellor before acting on anything here, and never change a prescribed medicine without your prescriber.