i5005436
A SNP in the CYP21A2 gene on chromosome 6. Its most notable genotype is C;T: miscalled by 23andMe, but should indicate being a carrier of allele for congenital adrenal hyperplasia
- Gene
- CYP21A2
- Location
- Chr 632,008,312 (GRCh38)
- Highest magnitude
- 3.0Important
- Tested on
- 23andMe
Genotypes
As shown in 23andMe and AncestryDNA files.
- C;CGoodnormal
- C;TMost notableBadmiscalled by 23andMe, but should indicate being a carrier of allele for congenital adrenal hyperplasia
On SNPedia: (C;C), (C;T). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Related
Conditions, medicines and genes
Other CYP21A2 SNPs
- rs6445T;TCongenital adrenal hyperplasiaVery important
- rs6471T;TCongenital adrenal hyperplasiaVery important
- rs6475A;ACongenital adrenal hyperplasiaVery important
- rs6476A;ACongenital adrenal hyperplasiaVery important
- rs7755898T;TCongenital adrenal hyperplasiaVery important
- rs151344503A;ACongenital adrenal hyperplasiaVery important
- rs151344505A;ACongenital adrenal hyperplasiaVery important
- rs201552310A;ACongenital adrenal hyperplasiaVery important
Notes
From SNPedia
Notes
Congenital adrenal hyperplasia rs7769409
C;T
As with rs7755898(C;T), for 23andMe users this commonly occurs as the result of a genotyping error in that testing platform. This can be seen in the opensnp data. If you were tested on another platform this may be real and further testing is perhaps warranted. See discussion at Congenital adrenal hyperplasia
Source and license
Adapted from i5005436 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.