Bibliome.ai browser hg19
Search
About
Stats
FAQ
FOXP2 c.1770-316G>T
Variant ID: 7-114303189-G-T
NM_014491.3(
FOXP2
):c.1770-316G>T
This variant was identified in 1 publication
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Genetic modifiers of Hb E/beta0 thalassemia identified by a two-stage genome-wide association study.
Bmc Medical Genetics
Sherva, Richard R; Sripichai, Orapan O; Abel, Kenneth K; Ma, Qianli Q; Whitacre, Johanna J; Angkachatchai, Vach V; Makarasara, Wattanan W; Winichagoon, Pranee P; Svasti, Saovaros S; Fucharoen, Suthat S; Braun, Andreas A; Farrer, Lindsay A LA
Publication Date: 2010-03-30
Variant appearance in text: rs1563408
PubMed Link:
20353593
Variant Present in the following documents:
Main text
1471-2350-11-51.pdf
View BVdb publication page