rs2235067
A SNP in the ABCB1 gene on chromosome 7. Its most notable genotype is T;T.
- Gene
- ABCB1
- Location
- Chr 787,520,606 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 12%
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
- T;TMost notableNot ratedNo summary available.
- C;TNot ratedNo summary available.
- C;CNot ratedNo summary available.
SNPedia records rs2235067 on the minus strand: (A;A), (A;G), (G;G). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Frequency
Share of each genotype in 11 HapMap populations.
- AverageT;T 2% C;T 22% C;C 76%
- European ancestry (Utah)T;T <1% C;T 27% C;C 72%
- Han Chinese (Beijing)T;T 0% C;T 10% C;C 91%
- Japanese (Tokyo)T;T 2% C;T 16% C;C 82%
- Yoruba (Nigeria)T;T 8% C;T 33% C;C 59%
- African ancestry (Southwest US)T;T 5% C;T 28% C;C 67%
- Chinese (Denver)T;T 0% C;T 6% C;C 94%
- Gujarati IndianT;T 0% C;T 29% C;C 71%
- Luhya (Kenya)T;T 4% C;T 26% C;C 71%
- Mexican ancestry (Los Angeles)T;T 0% C;T 21% C;C 79%
- Maasai (Kenya)T;T 6% C;T 22% C;C 72%
- TuscanT;T 2% C;T 25% C;C 74%
Related
Conditions, medicines and genes
Other ABCB1 SNPs
- rs1045642A;Aaltered drug metabolism and bioavailability; moderately increased risk for certain cancersImportant
- rs2032582T;Trare genotype, on a triallelic snpMinor
- rs2235040T;Tpossibly higher chances of remission only for inpatients on certain antidepressantsMinor
- rs10248420A;Apossibly less likely to remit on certain antidepressantsMinor
- rs4148739C;Tpossibly, inpatients more likely to remit on certain antidepressantsMinor
- rs3842T;TNo summary available.Typical
- rs1128503G;GnormalTypical
- rs2032583G;GNo summary available.Typical
Notes
From SNPedia
Show notes, about 310 words
rs2235067 is a SNP in the ABCB1 gene (also known as the MDR1 gene), which encodes a protein that transports certain molecules across the blood-brain barrier. SNPs in ABCB1 may thus influence the intracerebral concentrations of certain drugs and their efficacy or potential for adverse side effects. However, the link between the increased brain concentrations of antidepressants and a clinically significant response is unconfirmed. In clinic, even the lower concentrations of drugs may achieve sufficient antidepressant effect, and the dose of the drug can be adjusted upwards until the patient responds. According to a recent review , ten studies reported that ABCB1 SNPs have clinical effect in depression and eight that they do not. rs2235067 is one of 9 SNPs found within a tight linkage block (r 2 >= 0.8 ) such that the minor allele at any one of them predicts (with ~80%+ accuracy) that the other SNPs will also be the minor allele. The list of the 9 SNPs is shown below. When treated for depression with citalopram, paroxetine, amitriptyline, or venlafaxine (substrates of the protein encoded by ABCB1), a highly statistically significant association between the overall genetic variability of these SNPs and the remission was reported by Uhr et al in a study of ~400 German inpatients. However, the result for rs2235067 has to be treated with caution. A well-run, double-blind study of ABCB1 substrate citalopram in depression (STAR-D study) and a following meta-analysis failed to replicate several Uhr et al. results for other ABCB1 SNPs in this block. The 9 SNPs in the linkage block identified are : * rs2235067 * rs4148740 * rs2032583 * rs4148739 * rs11983225 * rs2235040 * rs12720067 * rs7787082 * rs10248420 ABCB1 (MDR1) genetic variants are associated with methadone doses required for effective treatment of heroin dependence.
Source and license
Adapted from rs2235067 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.