Variant ID: 10-114914913-T-G

NM_030756.4(TCF7L2):c.1200+2714T>G

This variant was identified in 2 publications




Publications:


Genome-wide significant associations for variants with minor allele frequency of 5% or less--an overview: A HuGE review.

American Journal Of Epidemiology
OA Panagiotou, E Evangelou, JP Ioannidis
Publication Date: 2010-10-15

Variant appearance in text: rs10509970
PMID: 20876667
View BVdb publication page



Genome-wide association with diabetes-related traits in the Framingham Heart Study.

Bmc Medical Genetics
JB Meigs, AK Manning, CS Fox, JC Florez, C Liu, LA Cupples, J Dupuis
Publication Date: 2007-09-19

Variant appearance in text: rs10509970
PMID: 17903298
View BVdb publication page



Alternative transcript annotations:

Transcript cDNA Protein Consequence Exon Intron
ENST00000277945.7 c.420+2714T>G - intron_variant - 4/6
ENST00000352065.5 c.1200+2714T>G - intron_variant - 10/14
ENST00000355717.4 c.1341+2714T>G - intron_variant - 11/12
ENST00000355995.4 c.1269+2714T>G - intron_variant - 11/14
ENST00000369386.1 c.198+2714T>G - intron_variant - 3/6
ENST00000369389.1 c.402+2714T>G - intron_variant - 5/6
ENST00000369397.4 c.1200+2714T>G - intron_variant - 10/13
ENST00000466338.1 n.222+2714T>G - intron_variant,non_coding_transcript_variant - 2/3
ENST00000470254.1 c.162+2714T>G - intron_variant,NMD_transcript_variant - 2/6
ENST00000480888.1 n.27+2714T>G - intron_variant,non_coding_transcript_variant - 1/2
ENST00000534894.1 c.1269+2714T>G - intron_variant - 11/14
ENST00000536810.1 c.1269+2714T>G - intron_variant - 11/13
ENST00000538897.1 c.1269+2714T>G - intron_variant - 11/13
ENST00000542695.1 c.417+2714T>G - intron_variant - 11/14
ENST00000543371.1 c.1269+2714T>G - intron_variant - 11/13
ENST00000545257.1 c.1269+2714T>G - intron_variant - 11/14
NM_001146274.2 c.1269+2714T>G - intron_variant - 11/13
NM_001146283.2 c.1341+2714T>G - intron_variant - 11/12
NM_001146284.2 c.1188+2714T>G - intron_variant - 10/12
NM_001146285.1 c.1200+2714T>G - intron_variant - 10/12
NM_001146286.2 c.1200+2714T>G - intron_variant - 10/11
NM_001198525.2 c.1215+2714T>G - intron_variant - 10/14
NM_001198526.2 c.1200+2714T>G - intron_variant - 10/12
NM_001198527.2 c.1188+2714T>G - intron_variant - 10/14
NM_001198528.2 c.1200+2714T>G - intron_variant - 10/14
NM_001198529.2 c.1200+2714T>G - intron_variant - 10/12
NM_001198530.1 c.1098+2714T>G - intron_variant - 9/10
NM_001198531.2 c.1269+2714T>G - intron_variant - 11/12
NM_001349870.2 c.840+2714T>G - intron_variant - 7/11
NM_001349871.1 c.720+2714T>G - intron_variant - 7/11
NM_001363501.1 c.1269+2714T>G - intron_variant - 11/13
NM_001367943.1 c.1269+2714T>G - intron_variant - 11/14
NM_030756.5 c.1200+2714T>G - intron_variant - 10/13