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INPP5D c.663+3725A>G
Variant ID: 2-233999081-A-G
NM_001017915.1(
INPP5D
):c.663+3725A>G
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:
Early Life Adversity and Polygenic Risk for High Fasting Insulin Are Associated With Childhood Impulsivity.
Frontiers In Neuroscience
Batra, Aashita A; Chen, Lawrence M LM; Wang, Zihan Z; Parent, Carine C; Pokhvisneva, Irina I; Patel, Sachin S; Levitan, Robert D RD; Meaney, Michael J MJ; Silveira, Patricia Pelufo PP
Publication Date: 2021
Variant appearance in text: rs11693862
PubMed Link:
34539334
Variant Present in the following documents:
Main text
fnins-15-704785.pdf
View BVdb publication page
Data on a genome-wide association study of type 2 diabetes in a Maya population.
Data In Brief
Totomoch-Serra, Armando A; Domínguez-Cruz, Miriam Givisay MG; Muñoz, María de Lourdes ML; García-Escalante, María Guadalupe MG; Burgueño, Juan J; Díaz-Badillo, Álvaro Á; Valadez-González, Nina N; Escalante, Doris Pinto DP
Publication Date: 2020-02
Variant appearance in text: rs11693862
PubMed Link:
31872004
Variant Present in the following documents:
Main text
View BVdb publication page