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RNF130 c.693+7965C>T
Variant ID: 5-179432096-G-A
NM_018434.5(
RNF130
):c.693+7965C>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:
Association of genetic polymorphisms of PCSK9 with type 2 diabetes in Uygur Chinese population.
Bmc Cardiovascular Disorders
Wang, Meng-Meng MM; Lu, Chen-Fei CF; Yan, Shi-Qi SQ; Wang, Bao-Zhu BZ; Yesitayi, Gulinazi G; Tian, Yong-Liang YL; Xiang-Ma, ; Ma, Yi-Tong YT
Publication Date: 2022-06-22
Variant appearance in text: rs248320
PubMed Link:
35733117
Variant Present in the following documents:
Main text
12872_2022_Article_2710.pdf
View BVdb publication page