rs111033563
A SNP in the LOC108783645 gene on chromosome 6. Its most notable genotype is A;C: Carrier of a hemochromatosis variant
- Gene
- LOC108783645
- Location
- Chr 626,092,916 (GRCh38)
- Highest magnitude
- 3.0Important
- Tested on
- AncestryDNA
Genotypes
As shown in 23andMe and AncestryDNA files.
- A;AGoodcommon in clinvar
- A;CMost notableBadCarrier of a hemochromatosis variant
On SNPedia: (A;A), (A;C). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Related
Other LOC108783645 SNPs
- rs1800562A;ATwo copies of C282Y, likely affected by hemochromatosis which may be serious if male or post-menopausal.Very important
- rs1799945G;GTwo copies of H63D, likely affected by mild form of hemochromatosisVery important
- rs28934595A;CCarrier of a hemochromatosis variantImportant
- rs28934596C;TCarrier of a hemochromatosis variantImportant
- rs28934597C;GCarrier of a hemochromatosis variantImportant
- rs146519482G;TCarrier of a hemochromatosis variantImportant
- rs797045145A;GCarrier of a hemochromatosis variantImportant
- rs1800730T;Taffected by a mild form of hemochromatosisWorth knowing
Notes
From SNPedia
Notes
A;C
Unaffected in absence of a second HFE gene mutation
Source and license
Adapted from rs111033563 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.