rs2630578

A SNP in the BICD1 gene on chromosome 12. Its most notable genotype is G;G: common in complete genomics

Gene
BICD1
Location
Chr 1232,152,853 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, AncestryDNA
Minor allele frequency
15%

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. G;GMost notableGoodcommon in complete genomicsTypical · 0.072% of people

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

Frequency

Share of each genotype in 11 HapMap populations.

  • AverageG;G 72%
  • European ancestry (Utah)G;G 66%
  • Han Chinese (Beijing)G;G 56%
  • Japanese (Tokyo)G;G 67%
  • Yoruba (Nigeria)G;G 89%
  • African ancestry (Southwest US)G;G 70%
  • Chinese (Denver)G;G 61%
  • Gujarati IndianG;G 73%
  • Luhya (Kenya)G;G 85%
  • Mexican ancestry (Los Angeles)G;G 86%
  • Maasai (Kenya)G;G 67%
  • TuscanG;G 69%

Notes

From SNPedia

Show notes, about 210 words

An association regarding telomere length with a p-value of (1.9x10^(-5)), stated that people carrying the minor allele 'C' at rs2630578 have telomeres within their white blood cells (leukocytes) that are on average 604 (+/-204) base pairs shorter than people who carry the common 'GG' genotype at this SNP. The authors estimate that this size of a difference between telomere length is equivalent to having cells which have comparatively gone through an additional "15-20 years of age-related attrition", however, no actual effects on aging or health were associated with this SNP in the study. As rs2630578 was genotyped by both the v3 & v4 chips, it should be in 23andMe's database for the majority of their customers, however, if this specific location was not genotyped or returned a 'No Call' or similar non-result - it may still be possible to determine your genotype by using the direct substitute rs2668301. This is possible because, as made apparent by comparing the population frequencies of the two SNPs, they are in very close linkage with one another within most human populations. Meaning, the 'T' version of rs2668301 is equivalent to having the 'G' version of rs2630578, and the 'C' alleles for both SNPs are equivalent to each other.)

Source and license

Adapted from rs2630578 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.