rs1544410 - GET-Evidence


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Short summary

rs1544410 is a Vitamin D Receptor (VDR) single nucleotide polymorphism. It is unlikely that it has functional significance because it is located in an intron (Liu et. al.), but it is in strong linkage disequilibrium with rs731236 (Dvornyk et al), which is located in an exon.

Variant evidence
Functional -1

This variant is located in a non-coding region of the genome, and it is unlikely that it has functional significance.

Clinical importance
Severity 1

Associated with an elevated risk of Type II Diabetes (see explanation below).


There are no known interventions.



Low clinical importance, Uncertain pharmacogenetic

(The "low clinical importance, uncertain" qualifier is assigned automatically based on the above evidence and importance scores.)

Inheritance pattern


Summary of published research, and additional commentary

This variant has been studied extensively. It has been linked to Type II Diabetes (Mukhopadhyaya et al). However, this study also linked rs731236 to the disease. Since rs731236 is located in an exon while rs1544410 is located in an intron, and the two variants are in strong linkage disequilibrium, it is likely that any functional effect comes from the other variant.

Dvornyk, V, JR Long, PY Liu, H Shen, RR Recker and HW Deng. “Polymorphisms of the vitamin D receptor gene predict the onset of surgical menopause in Caucasian females. .” Gynecol Endocrinol (2006): n. pag. Web. 3 Apr 2011.

Liu, Yao, Wei Chen, Zhi-bin Hu, Lin Xu, Yong-qian Shu, Shi-yang Pan Jun-Chang Dai, Guang-Fu Jin, Hong-zia Ma and Hong-bing Shen. “Plasma Vitamin D Levels And Vitamin D Receptor Polymorphisms Are Associated with Survival of Non-small Cell Lung Cancer.” Chin J Cancer Res (2011): n. pag. Web. 31 Mar 2011.

Mukhopadhyaya , P.N. , A, Acharya , Y. Chavan , S.S. Purohit , and A. Mutha. “Metagenomic study of single-nucleotide polymorphism within candidate genes associated with type 2 diabetes in an Indian population.” Genetics and Molecular Research 9.4 (2010): n. pag. Web. 3 Apr 2011.

Allele frequency

  • T @ chr12:46526101: 35.2% (45/128) in GET-Evidence
  • Frequency shown in summary reports: 35.2% (45/128)



hu034DB1 - CGI sample GS00253-DNA_A02_200_37
het T @ chr12:48239835


hu04FD18 - CGI sample GS00253-DNA_F01_200_37
het T @ chr12:48239835


hu0D879F - CGI sample GS00253-DNA_G01_200_37
het T @ chr12:48239835



hu43860C - CGI sample GS00253-DNA_A01_200_37
hom T @ chr12:48239835


hu604D39 - CGI sample GS00253-DNA_B02_200_37
het T @ chr12:48239835


hu9385BA - CGI sample GS00253-DNA_E01_200_37
het T @ chr12:48239835


huAE6220 - CGI sample GS00253-DNA_H01_200_37
het T @ chr12:48239835


huBEDA0B - CGI sample GS00253-DNA_C01_200_37
het T @ chr12:48239835


huC30901 - CGI sample GS00253-DNA_B01_200_37
het T @ chr12:48239835


huE80E3D - CGI sample GS00253-DNA_D01_200_37
hom T @ chr12:48239835


GS06985 - var-GS06985-1100-36-ASM
het T @ chr12:46526102


GS10851 - var-GS10851-1100-36-ASM
het T @ chr12:46526102


GS18502 - var-GS18502-1100-36-ASM
hom T @ chr12:46526102


GS18504 - var-GS18504-1100-36-ASM
het T @ chr12:46526102


GS18508 - var-GS18508-1100-36-ASM
hom T @ chr12:46526102


GS18517 - var-GS18517-1100-36-ASM
hom T @ chr12:46526102


GS18956 - var-GS18956-1100-36-ASM
het T @ chr12:46526102


GS19025 - var-GS19025-1100-36-ASM
het T @ chr12:46526102


GS19238 - var-GS19238-1100-36-ASM
het T @ chr12:46526102


GS19648 - var-GS19648-1100-36-ASM
het T @ chr12:46526102


GS19649 - var-GS19649-1100-36-ASM
het T @ chr12:46526102


GS19669 - var-GS19669-1100-36-ASM
het T @ chr12:46526102


GS19700 - var-GS19700-1100-36-ASM
het T @ chr12:46526102


GS19834 - var-GS19834-1100-36-ASM
het T @ chr12:46526102


GS20502 - var-GS20502-1100-36-ASM
het T @ chr12:46526102


GS20509 - var-GS20509-1100-36-ASM
het T @ chr12:46526102


GS21767 - var-GS21767-1100-36-ASM
het T @ chr12:46526102




Other external references

  • rs1544410

Other in silico analyses

  • GET-Evidence autoscore = 1

Edit history

Gene search

"GENE" or "GENE A123C":

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