rs1544410 - GET-Evidence

Note: This variant has not been sufficiently evaluated by a GET-Evidence editor.

To be considered sufficiently evaluated a variant must have both "variant evidence" and "clinical importance" scores filled in.

Please help improve GET-Evidence by evaluating evidence for this variant!

Curation:
Currentness:

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rs1544410


You are viewing an old version of this page that was saved on December 5, 2010 at 6:43pm by Genome Importing Robot.

Short summary

 

Variant evidence
Computational -
Functional -
Case/Control -
Familial -
 
Clinical importance
Severity -
Treatability -
Penetrance -
 

Impact

Insufficiently evaluated pharmacogenetic

(The "insufficiently evaluated" qualifier is assigned automatically based on the above evidence and importance scores.)

Inheritance pattern

unknown

Summary of published research, and additional commentary

 

Allele frequency

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

Publications
 

Genomes
 

Added in this revision:

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

 

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

 

hu9385BA - CGI sample GS00253-DNA_E01_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

 

snp-18

 

snp-26

 

snp-32

 

Other external references
 

    dbSNP
  • rs1544410
    www.ncbi.nlm.nih.gov/projects/SNP/snp_ref.cgi

Other in silico analyses
 

  • GET-Evidence autoscore = 1

Edit history
 

Gene search

"GENE" or "GENE A123C":

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