rs150504822
A SNP in the SLITRK1 gene on chromosome 13. Its most notable genotype is A;T: Likely miscall in 23andMe v5 data; otherwise, association with OCD
- Gene
- SLITRK1
- Location
- Chr 1383,880,256 (GRCh38)
- Highest magnitude
- 5.0Very important
- Tested on
- 23andMe
Genotypes
As shown in 23andMe and AncestryDNA files.
- A;TMost notableBadLikely miscall in 23andMe v5 data; otherwise, association with OCD
- T;TGoodcommon/normal
On SNPedia: (A;T), (T;T). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Related
Other SLITRK1 SNPs
- rs191284403C;TReported in association with Tourette's and trichotillomaniaVery important
- rs193302861-;GReported in association with Tourette's and trichotillomaniaVery important
- rs1035448844C;TReported to be associated with Tourette's and trichotillomaniaVery important
- rs1368546312C;TReported to be associated with Tourette's and trichotillomaniaVery important
Notes
From SNPedia
Notes
aka c.1252A>T (p.Thr418Ser or T418S); note ambiguous flip potential, especially given plus/FWD orientation of SNP but minus/REV orientation of cDNA
A;T
see links via main rs-page and to SLITRK1 gene
Source and license
Adapted from rs150504822 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.