rs6511720
A SNP in the LDLR gene on chromosome 19. Its most notable genotype is G;T: Slightly lower odds of developing CHD.
- Gene
- LDLR
- Location
- Chr 1911,091,630 (GRCh38)
- Highest magnitude
- 2.0Worth knowing
- Tested on
- 23andMe, AncestryDNA
- Minor allele frequency
- 8%
Genotypes
As shown in 23andMe and AncestryDNA files.
- G;GGoodcommon in complete genomics
- G;TMost notableGoodSlightly lower odds of developing CHD.
- T;TGoodSlightly lower odds of developing CHD.
On SNPedia: (G;G), (G;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.
- AverageG;G 82% G;T 16% T;T 2%
- European ancestry (Utah)G;G 81% G;T 16% T;T 3%
- Han Chinese (Beijing)G;G 100% G;T 0% T;T 0%
- Japanese (Tokyo)G;G 100% G;T 0% T;T 0%
- Yoruba (Nigeria)G;G 73% G;T 24% T;T 3%
- African ancestry (Southwest US)G;G 77% G;T 19% T;T 4%
- Chinese (Denver)G;G 98% G;T 2% T;T 0%
- Gujarati IndianG;G 83% G;T 17% T;T 0%
- Luhya (Kenya)G;G 71% G;T 28% T;T 2%
- Mexican ancestry (Los Angeles)G;G 85% G;T 14% T;T 2%
- Maasai (Kenya)G;G 61% G;T 33% T;T 6%
- TuscanG;G 78% G;T 20% T;T 2%
Related
Other LDLR SNPs
- rs121908027-;-familial hypercholesterolemiaVery important
- rs5933C;GFamilial HypercholesterolemiaVery important
- rs2228671A;CFamilial HypercholesterolemiaVery important
- rs2569548C;TFamilial HypercholesterolemiaVery important
- rs11547917A;CFamilial HypercholesterolemiaVery important
- rs13306512A;CFamilial HypercholesterolemiaVery important
- rs13306515A;CFamilial HypercholesterolemiaVery important
- rs28941776A;GFamilial HypercholesterolemiaVery important
Source and license
Adapted from rs6511720 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.