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THSD7A c.3538-1048G>A
Variant ID: 7-11453475-C-T
NM_015204.2(
THSD7A
):c.3538-1048G>A
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:
Estimating the Prevalence and Genetic Risk Mechanisms of ARFID in a Large Autism Cohort.
Frontiers In Psychiatry
Koomar, Tanner T; Thomas, Taylor R TR; Pottschmidt, Natalie R NR; Lutter, Michael M; Michaelson, Jacob J JJ
Publication Date: 2021
Variant appearance in text: rs78495856
PubMed Link:
34177659
Variant Present in the following documents:
Main text
fpsyt-12-668297.pdf
View BVdb publication page