rs387907200
A SNP in the SPR gene on chromosome 2. Its most notable genotype is G;T: Carrier of a SPR deficiency mutation
- Gene
- SPR
- Location
- Chr 272,887,736 (GRCh38)
- Highest magnitude
- 3.0Important
- Tested on
- AncestryDNA
Genotypes
As shown in 23andMe and AncestryDNA files.
- G;GGoodcommon in clinvar
- G;TMost notableBadCarrier of a SPR deficiency mutation
On SNPedia: (G;G), (G;T). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Related
Other SPR SNPs
- rs104893665A;GCarrier of a SPR deficiency mutationImportant
- rs104893666C;TCarrier of a SPR deficiency mutationImportant
- rs121917746C;TCarrier of a SPR deficiency mutationImportant
- rs121917747A;TCarrier of a SPR deficiency mutationImportant
- rs398122922A;GCarrier of a SPR deficiency mutationImportant
- rs587776777-;AGAACCarrier of a SPR deficiency mutationImportant
Notes
From SNPedia
Notes
aka c.304G>T (p.Gly102Cys)
G;T
Unaffected in absence of a second mutation in the SPR gene; see links via main rs-page.
Source and license
Adapted from rs387907200 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.