rs2900492
A SNP in the ABCC9 gene on chromosome 12. Its most notable genotype is A;A: common in complete genomics
- Gene
- ABCC9
- Location
- Chr 1221,889,314 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- FamilyTreeDNA
- Minor allele frequency
- 2%
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (A;A). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Frequency
Share of each genotype in 4 HapMap populations.
- AverageA;A 99%
- European ancestry (Utah)A;A 95%
- Han Chinese (Beijing)A;A 100%
- Japanese (Tokyo)A;A 100%
- Yoruba (Nigeria)A;A 100%
Related
Notes
From SNPedia
Notes
Genes controlling postural changes in blood pressure: comprehensive association analysis of ATP-sensitive potassium channel genes KCNJ8 and ABCC9. rs2900492(G) associated with postural changes in blood pressure. Also in haplotypes rs2900492(A)-rs2955503(A) and rs2900492(G)-rs11046232(A)-rs4148649(A)-rs4762865(A) associated with postural changes in blood pressure.
Source and license
Adapted from rs2900492 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.