rs3208363
A SNP in the CYP3A4 gene on chromosome 7. Its most notable genotype is C;C: CYP3A4*_16907T>G(S252A) homozygote
- Gene
- CYP3A4
- Location
- Chr 799,767,175 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
- C;CMost notableNot ratedCYP3A4*_16907T>G(S252A) homozygote
- A;CNot ratedcarrier of one CYP3A4*_16907T>G(S252A) allele
- A;AGoodnormal
SNPedia records rs3208363 on the minus strand: (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 10 HapMap populations.
- AverageC;C <1% A;C 1% A;A 99%
- European ancestry (Utah)C;C 0% A;C 0% A;A 100%
- Han Chinese (Beijing)C;C 0% A;C 0% A;A 100%
- Japanese (Tokyo)C;C 0% A;C 0% A;A 100%
- Yoruba (Nigeria)C;C 0% A;C 0% A;A 100%
- African ancestry (Southwest US)C;C 0% A;C 5% A;A 95%
- Chinese (Denver)C;C 0% A;C 1% A;A 99%
- Gujarati IndianC;C 0% A;C 1% A;A 99%
- Luhya (Kenya)C;C <1% A;C 2% A;A 97%
- Mexican ancestry (Los Angeles)C;C 0% A;C 2% A;A 98%
- TuscanC;C 0% A;C 1% A;A 99%
Related
Other CYP3A4 SNPs
- rs67666821T;TCYP3A4*20 homozygote; side effects likely from many drugsVery important
- rs12721629A;ACYP3A4*12 homozygoteWorth knowing
- rs1041988G;GCYP3A4*_23139T>C(I431T) homozygoteTypical
- rs2242480C;CnormalTypical
- rs3091339T;TnormalTypical
- rs3208361T;TnormalTypical
- rs4646437G;Gcommon in complete genomicsTypical
- rs4646440G;Gcommon in complete genomicsTypical
Notes
From SNPedia
Notes
rs3208363 is a SNP in the CYP3A4 gene. The rs3208363(G) allele defines the CYP3A4*_16907T>G(S252A) variant.
Source and license
Adapted from rs3208363 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.