rs6476

A SNP in the CYP21A2 gene on chromosome 6. Its most notable genotype is A;A: Congenital adrenal hyperplasia

Gene
CYP21A2
Location
Chr 632,039,816 (GRCh38)
Highest magnitude
5.0Very important
Tested on
23andMe, AncestryDNA
Minor allele frequency
<1%

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. A;AMost notableBadCongenital adrenal hyperplasiaVery important · 5.00% of people
  2. A;TBadCarrier of allele for congenital adrenal hyperplasiaImportant · 3.01% of people
  3. T;TGoodcommon in clinvarTypical · 0.099% of people

On SNPedia: (A;A), (A;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 4 HapMap populations.

  • AverageA;A 0% A;T 1% T;T 99%
  • European ancestry (Utah)A;A 0% A;T 0% T;T 100%
  • Han Chinese (Beijing)A;A 0% A;T 0% T;T 100%
  • Japanese (Tokyo)A;A 0% A;T 2% T;T 98%
  • Yoruba (Nigeria)A;A 0% A;T 2% T;T 98%

Conditions, medicines and genes

Notes

From SNPedia

Notes

A;A

See discussion at Congenital adrenal hyperplasia

A;T

See discussion at Congenital adrenal hyperplasia

Source and license

Adapted from rs6476 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.