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MMP2 c.529+182C>T
Variant ID: 16-55518258-C-T
NM_004530.4(
MMP2
):c.529+182C>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:
Evaluation of MMP2 as a candidate gene for high myopia.
Molecular Vision
Gong, Bo B; Liu, Xiaoqi X; Zhang, Dingding D; Wang, Pu P; Huang, Lulin L; Lin, Ying Y; Lu, Fang F; Ma, Shi S; Cheng, Jing J; Chen, Rong R; Li, Xiaobo X; Lin, He H; Zeng, Guangqun G; Zhu, Xiong X; Hu, Jianbin J; Yang, Zhenglin Z; Shi, Yi Y
Publication Date: 2013
Variant appearance in text: rs11076101
PubMed Link:
23378725
Variant Present in the following documents:
Main text
mv-v19-121.pdf
View BVdb publication page