Bibliome.ai browser hg19
Search
About
Stats
FAQ
ZNF385B c.-155+10122A>T
Variant ID: 2-180715706-T-A
NM_152520.6(
ZNF385B
):c.-155+10122A>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 Studies of Hypertension and Several Other Cardiovascular Diseases.
Pulse (Basel, Switzerland)
Wang, Yan Y; Wang, Ji-Guang JG
Publication Date: 2019-04
Variant appearance in text: rs13407401
PubMed Link:
31049317
Variant Present in the following documents:
Main text
View BVdb publication page
Brief Overview of a Decade of Genome-Wide Association Studies on Primary Hypertension.
International Journal Of Endocrinology
Azam, Afifah Binti AB; Azizan, Elena Aisha Binti EAB
Publication Date: 2018
Variant appearance in text: rs13407401
PubMed Link:
29666641
Variant Present in the following documents:
Main text
IJE2018-7259704.pdf
View BVdb publication page