rs6311
A SNP in the HTR2A gene on chromosome 13. Its most notable genotype is C;C: 3.6x increased risk of sexual dysfunction when taking SSRI Antidepressants.
- Gene
- HTR2A
- Location
- Chr 1346,897,343 (GRCh38)
- Highest magnitude
- 3.0Important
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 44%
Genotypes
As shown in 23andMe and AncestryDNA files.
- C;CMost notableBad3.6x increased risk of sexual dysfunction when taking SSRI Antidepressants.
- C;TGoodNormal risk of sexual dysfunction when taking SSRI Antidepressants.
- T;TGoodNormal (lower) risk of sexual dysfunction when taking SSRI Antidepressants.
On SNPedia: (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 11 HapMap populations.
- AverageC;C 31% C;T 49% T;T 19%
- European ancestry (Utah)C;C 27% C;T 52% T;T 20%
- Han Chinese (Beijing)C;C 22% C;T 45% T;T 33%
- Japanese (Tokyo)C;C 24% C;T 50% T;T 26%
- Yoruba (Nigeria)C;C 40% C;T 46% T;T 14%
- African ancestry (Southwest US)C;C 32% C;T 47% T;T 21%
- Chinese (Denver)C;C 14% C;T 55% T;T 31%
- Gujarati IndianC;C 38% C;T 50% T;T 13%
- Luhya (Kenya)C;C 44% C;T 45% T;T 12%
- Mexican ancestry (Los Angeles)C;C 36% C;T 52% T;T 12%
- Maasai (Kenya)C;C 47% C;T 46% T;T 7%
- TuscanC;C 23% C;T 53% T;T 25%
Related
Conditions, medicines and genes
Other HTR2A SNPs
- rs6313A;Adepression, panic, stress responseWorth knowing
- rs6314G;Ghigher risk for RATypical
- rs594242C;GNo summary available.Typical
- rs643627A;GNo summary available.Typical
- rs659734A;Acommon in complete genomicsTypical
- rs1328674T;Thigher risk for RATypical
- rs2224721G;Gcommon/normalTypical
- rs7997012A;A~18% more likely to respond to citalopramTypical
Genosets
- Gs108Rheumatoid arthritis riskWorth knowing
- Gs109Rheumatoid arthritis risk; more stringent form of Gs108Worth knowing
Genosets combine several genotypes. Twofold checks them in your report.
Notes
From SNPedia
Show notes, about 310 words
rs6311 (-1438A>G / A-1438G or -1438G>A / G-1438A) is a SNP located upstream (and within the promoter region) of HTR2A. Multiple Regulatory Variants Modulate Expression of 5-Hydroxytryptamine 2A Receptors in Human Cortex. The minor A allele of rs6311 reduces expression of a previously unannotated extension of the 5' untranslated region of HTR2A mRNA. rs6311 together with rs6314 have a modest effect on depression severity, when examined in the Sequenced Treatment Alternatives to Relieve Depression (STAR*D) study. Three (rs643627-rs594242-rs6311: A-C-T), two (rs594242-rs6311: C-T) and a single functional (rs6311: T) marker were protective against suicidal behavior. The complementary markers (rs594242-rs6311: G-C and rs6311: C) were associated with increased risk for non-violent and impulsive suicidal behavior. Furthermore, CC-homozygotes for the functional SNP rs6311 reported more anger- and aggression-related behavior. This SNP has also been reported to be part of a haplotype associated with risk for rheumatoid arthritis. In this report, the risk allele is rs6311(C). may effect promoter activity (in the presence of a SV40 enhancer, promoter activity was significantly higher with the A allele than a G allele, but only in cell lines expressing endogenous HTR2A) -1438 A allele creates a consensus binding site for Th1/E47, a transcription factor implicated in development of the nervous system Polymorphisms in the serotonin receptor gene HTR2A are associated with quantitative traits in panic disorder.
C;C
Selective Seratonin Reuptake Inhibitors (citalopram (Celexa), escitalopram (Lexapro), fluoxetine (Prozac), paroxetine (Paxil), or sertraline (Zoloft)) cause worse sexual dysfunction (a common side-effect) in people with this SNP. Note that research has shown Saffron is effective at reversing the sexual dysfunction from SSRI anti-depressants.
References
Source and license
Adapted from rs6311 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.