rs4844614
A SNP in the CR1L gene on chromosome 1. Its most notable genotype is G;G.
- Gene
- CR1L
- Location
- Chr 1207,701,830 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA
- Minor allele frequency
- 33%
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (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.
- AverageG;G 49%
- European ancestry (Utah)G;G 62%
- Han Chinese (Beijing)G;G 34%
- Japanese (Tokyo)G;G 30%
- Yoruba (Nigeria)G;G 50%
- African ancestry (Southwest US)G;G 56%
- Chinese (Denver)G;G 47%
- Gujarati IndianG;G 43%
- Luhya (Kenya)G;G 60%
- Mexican ancestry (Los Angeles)G;G 26%
- Maasai (Kenya)G;G 70%
- TuscanG;G 61%
Related
Conditions, medicines and genes
Notes
From SNPedia
Show notes, about 120 words
per the 23andMe blog, the minor allele of this SNP (T) was associated with increased LDL cholesterol {| border="1" |- !SNP !Rarer allele !LDL !HDL !TG |- | rs6544713 || T || + || || |- | rs2650000 || A || + || || |- | rs471364 || C || || - || |- | rs1800961 || T || || - || |- | rs7679 || C || || - || + |- | rs2967605 || T || || - || |- | rs2409722 || T || || || - |- | rs10903129 || A || - || - || - |- | rs6756629 || A || - || + || - |- | rs12670798 || C || + || + || + |- | rs7395662 || A || - || + || + |- | rs174570 || T || - || - || + |- | rs2271293 || A || - || + || - |- | rs2624265 || C || || || + |- | rs2167079 || T || || + || |- | rs9891572 || T || || + || |- | rs4844614 || T || + || || |- | rs5031002 || G || + || || |- |}
Source and license
Adapted from rs4844614 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.