Bibliome.ai browser hg19
Search
About
Stats
FAQ
NDUFA13 c.94+896G>A
Variant ID: 19-19628037-G-A
NM_015965.6(
NDUFA13
):c.94+896G>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:
Genetic Overlap Analysis Identifies a Shared Etiology between Migraine and Headache with Type 2 Diabetes.
Genes
Islam, Md Rafiqul MR; The International Headache Genetics Consortium Ihgc, ; Nyholt, Dale R DR
Publication Date: 2022-10-12
Variant appearance in text: rs7252888
PubMed Link:
36292730
Variant Present in the following documents:
genes-13-01845.pdf
View BVdb publication page