PTCH1
87 SNPs in the PTCH1 gene, 17 with a genotype of magnitude 2 or higher.
- Type
- Gene
- SNPs
- 87
- Notable
- 17Magnitude 2 or higher
- Well documented
- 4
- Genosets
- 0
PTCH1 SNPs
Every genotype, as shown in 23andMe and AncestryDNA files.
- rs357564Typical
- rs473902Typical
- rs2066836Typical
- rs2236405Typical
- rs199476090Very important
- rs766313615Very important
- rs778260156Very important
- rs786204056Very important
- rs863224442Very important
- rs863224443Very important
- rs863224444Very important
- rs863224484Very important
- rs863224485Very important
- rs863224486Very important
- rs863224487Very important
- rs863225467Very important
- rs864622212Very important
- rs864622374Very important
- rs878853849Very important
- rs878853852Very important
- rs878853856Very important
No matches.
Other SNPs
No notable genotype or detailed notes
Show 66 SNPs
- rs357565
- rs10512248
- rs28377268
- rs28936403
- rs138911275
- rs147067171
- rs199476091
- rs199476093
- rs267606984
- rs368417828
- rs368869806
- rs372027952
- rs587776689
- rs587778629
- rs747234651
- rs752765582
- rs755103500
- rs765371196
- rs772407797
- rs776154605
- rs779966690
- rs780378700
- rs780434261
- rs781768965
- rs794727242
- rs863224650
- rs863225054
- rs863225055
- rs864622293
- rs864622583
- rs869025270
- rs878853847
- rs886039540
- rs886039678
- rs886041943
- rs886043550
- rs1057518400
- rs1057518664
- rs1057520590
- rs1060502264
- rs1060502268
- rs1060502271
- rs1060502273
- rs1060502274
- rs1060502277
- rs1060502278
- rs1060502280
- rs1060502281
- rs1060502285
- rs1060502286
- rs1060502287
- rs1060502292
- rs1060502295
- rs1060502297
- rs1060502298
- rs1060502301
- rs1064793921
- rs1064793922
- rs1064793978
- rs1064793991
- rs1064794117
- rs1064794260
- rs1064795637
- rs1064796259
- rs1085307511
- rs1085307752
Source and license
Adapted from PTCH1 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.