i3002758

A SNP in the TTR gene on chromosome 18. Its most notable genotype is A;A: TTR-related Familial Amyloid Polyneuropathy

Gene
TTR
Location
Chr 1829,172,937 (GRCh38)
Highest magnitude
4.0Very important
Tested on
23andMe

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. A;AMost notableBadTTR-related Familial Amyloid PolyneuropathyVery important · 4.0
  2. A;GBadTTR-related Familial Amyloid PolyneuropathyVery important · 4.0
  3. G;GGoodNormalTypical · 0.0

On SNPedia: (A;A), (A;G), (G;G). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.

Notes

From SNPedia

Notes

TTR-Related Familial Amyloid Polyneuropathy Familial amyloid polyneuropathies are neurological conditions. https://www.23andme.com/you/journal/ttr_familial_amyloid_polyneuropathy/techreport/ rs28933979

A;A

The majority of people with this genotype develop the neurological condition known as TTR-related familial amyloid polyneuropathy by the time they are 80, although the age of onset varies.

A;G

The majority of people with this genotype develop the neurological condition known as TTR-related familial amyloid polyneuropathy by the time they are 80, although the age of onset varies.

Source and license

Adapted from i3002758 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.