i5005732
A SNP in the LOC100652810 gene on chromosome 5. Its most notable genotype is A;A: Spinal muscular atrophy
- Gene
- LOC100652810
- Location
- Chr 570,238,217 (GRCh38)
- Highest magnitude
- 6.0Very important
- Tested on
- 23andMe
Genotypes
As shown in 23andMe and AncestryDNA files.
- A;AMost notableBadSpinal muscular atrophy
- A;GBadcarrier of a spinal muscular atrophy disease allele
- G;GGoodcommon/normal
On SNPedia: (A;A), (A;G), (G;G). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Related
Conditions, medicines and genes
Other LOC100652810 SNPs
- i5005727T;TSpinal muscular atrophyVery important
- i5005728T;TSpinal muscular atrophyVery important
- i5005729G;GSpinal muscular atrophyVery important
- i5005733A;ASpinal muscular atrophyVery important
- i5005734A;ASpinal muscular atrophyVery important
- i5005735T;TSpinal muscular atrophyVery important
- i5005737G;GSpinal muscular atrophyVery important
- i5005738G;GSpinal muscular atrophyVery important
Notes
From SNPedia
Notes
spinal muscular atrophy - possible association, not confirmed
A;A
see rs# link at i5005732
A;G
see rs# link at i5005732
Source and license
Adapted from i5005732 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.