rs143383
A SNP in the GDF5 gene on chromosome 20. Its most notable genotype is A;A: 1.3x increased risk for osteoarthritis
- Gene
- GDF5
- Location
- Chr 2035,438,203 (GRCh38)
- Highest magnitude
- 1.8Minor
- Tested on
- 23andMe, AncestryDNA
- Minor allele frequency
- 46%
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
- G;GGoodnormal risk for osteoarthritis
- A;GBad1.1x increased risk for osteoarthritis
- A;AMost notableBad1.3x increased risk for osteoarthritis
SNPedia records rs143383 on the minus strand: (C;C), (C;T), (T;T). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Frequency
Share of each genotype in 4 HapMap populations.
- AverageG;G 29% A;G 31% A;A 40%
- European ancestry (Utah)G;G 11% A;G 43% A;A 46%
- Han Chinese (Beijing)G;G 5% A;G 35% A;A 61%
- Japanese (Tokyo)G;G 2% A;G 44% A;A 54%
- Yoruba (Nigeria)G;G 100% A;G 0% A;A 0%
Related
Conditions, medicines and genes
Notes
From SNPedia
Show notes, about 520 words
This SNP is associated with osteoarthritis (OA). It is located in the five prime untranslated region (5′UTR) of the gene encoding growth differentiation factor 5 (GDF5), a chondrogenic protein active from the embryonic stage onwards. GDF5 is also known as cartilage-derived morphogenetic protein 1 or BMP14. The risk allele T (+ 104T/C;rs143383) causes reduction of the GDF5 promoter sequence activity. Reduction of GDF5 in human cartilage of patients with OA by up to 27% has been observed ora.ox.ac.uk. This effect is influenced by a second SNP ( rs143384 , C/T ) in the same area. The C alleles of both SNPs form CpG dinucleotides. Demethylation of both SNP's increases GDF5 expression.hmg.oxfordjournals.org Thus the authors conclude that epigenetic manipulation offers options in developing therapies for OA. rs143383 showed significant association with hip osteoarthritis in two independent Japanese populations. It also showed association with knee osteoarthritis in Japanese and Chinese populations. is *not* a risk factor for osteoarthritis in Greek Caucasians A subsequent study showed that the same risk allele, rs143383(T), was (somewhat) associated with osteoarthritis in European populations. The odds ratio was 1.10 for the allele, 1.28 for carrier status (p=0.03, p=0.004, respectively). The (T) allele appears to make less GDF5 protein, which eventually renders an individual somewhat more susceptible to osteoarthritis. A meta-analysis combining data from 11,000+ individuals as well as both European and Asian populations found strong evidence (p < 0.0004) confirming increased risk for osteoarthritis from the rs143383(T) allele. The best model is a dominant one, and the odds ratio reported is 1.21 in general and 1.48 for the dominant model. Another meta-analysis of 14 studies concluded that rs143383 did indeed show significant association with osteoarthritis, at least for knee osteoarthritis, and probably for hand and hip (but to a lesser degree). The effect size wasn't large, though (odds ratio 1.15, CI: 1.09-1.22, p = 9.4 x 10e-7). A haplotype of rs143383 and rs6060369 can be defined, which also links osteoarthritis to height since rs6060369 was linked to height in a study ultimately involving over 28,000 individuals. The Medpage article on this finding notes that rs143383 was previously shown to be associated with increased risk for osteoarthritis and in this recent study it was significantly associated with shorter height in the initial scans, at p=2.70x10e-5. Note that the authors of refer to rs143383 in the opposite orientation compared to it's entry in dbSNP. A study of 338 Han Chinese children affected by congenital dysplasia of the hip revealed that rs143383(T) alleles conferred a 1.4x increased risk for the disorder, particularly in females (odds ratio 1.43, CI: 1.11 - 1.85, p = 0.0078). A study of 6,365 elderly Caucasian men and women observed significant association between rs143383 and osteoarthritis, height, bone size and fracture risk in women.
Source and license
Adapted from rs143383 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.