Sequencings

Markers / Gene

MTHFR

2 positions in this gene are readable from a home DNA test.

MTHFR C677T, and why it is oversold

rs1801133 · chr1:11,856,378 · G/A · evidence: established

This is the single most over-interpreted position in consumer genetics. It genuinely does reduce the activity of an enzyme in folate metabolism. What it does not do is most of what the internet says it does.

If you carryWhat it means
No copiesYou do not carry C677T
One copyYou carry one copy, which changes nothing in practice
Two copiesYou carry two copies, which is common and still changes little
Ancestry groupA (the effect version)
African9.0%
American47.4%
East Asian29.6%
European36.5%
South Asian11.9%

1000 Genomes Project phase 3, via Ensembl, retrieved 2026-09-23. These groupings are coarse and flatten a great deal of internal diversity, particularly within Africa. A variant being common somewhere tells you where a piece of your ancestry probably comes from, and nothing else.

Full detail on rs1801133

MTHFR A1298C

rs1801131 · chr1:11,854,476 · T/G · evidence: established

The second common MTHFR variant, usually reported alongside C677T. It reduces enzyme activity less than C677T does.

If you carryWhat it means
No copiesYou do not carry A1298C
One copyYou carry one copy, which changes nothing in practice
Two copiesYou carry two copies, which still changes very little
Ancestry groupG (the effect version)
African15.1%
American15.1%
East Asian21.9%
European31.3%
South Asian41.7%

1000 Genomes Project phase 3, via Ensembl, retrieved 2026-09-23. These groupings are coarse and flatten a great deal of internal diversity, particularly within Africa. A variant being common somewhere tells you where a piece of your ancestry probably comes from, and nothing else.

Full detail on rs1801131

Where this gene fits

If you have taken a home DNA test, these positions are already in your file.

Read my file