i5005430
A SNP in the CYP21A2 gene on chromosome 6. Its most notable genotype is A;G: Carrier of allele for congenital adrenal hyperplasia
- Gene
- CYP21A2
- Location
- Chr 632,008,696 (GRCh38)
- Highest magnitude
- 3.0Important
- Tested on
- 23andMe
Genotypes
As shown in 23andMe and AncestryDNA files.
- A;GMost notableBadCarrier of allele for congenital adrenal hyperplasia
On SNPedia: (A;G). 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 rs72552758
A;G
See discussion at Congenital adrenal hyperplasia
Source and license
Adapted from i5005430 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.