rs104894263
A SNP in the MEN1 gene on chromosome 11. Its most notable genotype is C;G: Multiple Endocrine Neoplasia Type 1
- Gene
- MEN1
- Location
- Chr 1164,809,695 (GRCh38)
- Highest magnitude
- 5.8Very important
- Tested on
- AncestryDNA
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
- G;GGoodcommon in clinvar
- C;GMost notableBadMultiple Endocrine Neoplasia Type 1
SNPedia records rs104894263 on the minus strand: (C;C), (C;G). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Related
Other MEN1 SNPs
- rs104894256A;CMultiple Endocrine Neoplasia Type 1Very important
- rs104894258C;TMultiple Endocrine Neoplasia Type 1Very important
- rs104894259A;TMultiple Endocrine Neoplasia Type 1Very important
- rs104894260C;TMultiple Endocrine Neoplasia Type 1Very important
- rs104894261A;GMultiple Endocrine Neoplasia Type 1Very important
- rs104894262A;TMultiple Endocrine Neoplasia Type 1Very important
- rs104894265G;TMultiple Endocrine Neoplasia Type 1Very important
- rs104894266A;GMultiple Endocrine Neoplasia Type 1Very important
Source and license
Adapted from rs104894263 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.