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THSD7A c.1823-6891G>T
Variant ID: 7-11528500-C-A
NM_015204.2(
THSD7A
):c.1823-6891G>T
This variant was identified in 2 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Genome-wide association with bone mass and geometry in the Framingham Heart Study.
Bmc Medical Genetics
Kiel, Douglas P DP; Demissie, Serkalem S; Dupuis, Josée J; Lunetta, Kathryn L KL; Murabito, Joanne M JM; Karasik, David D
Publication Date: 2007-09-19
Variant appearance in text: rs10486135
PubMed Link:
17903296
Variant Present in the following documents:
Main text
View BVdb publication page
A genome-wide association for kidney function and endocrine-related traits in the NHLBI's Framingham Heart Study.
Bmc Medical Genetics
Hwang, Shih-Jen SJ; Yang, Qiong Q; Meigs, James B JB; Pearce, Elizabeth N EN; Fox, Caroline S CS
Publication Date: 2007-09-19
Variant appearance in text: rs10486135
PubMed Link:
17903292
Variant Present in the following documents:
Main text
1471-2350-8-S1-S10.pdf
View BVdb publication page