Bibliome.ai browser hg19
Search
About
Stats
FAQ
PTEN c.165-7883T>C
Variant ID: 10-89677387-T-C
NM_000314.4(
PTEN
):c.165-7883T>C
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:
No association between polymorphisms in PTEN and primary ovarian insufficiency in a Han Chinese population.
Reproductive Biology And Endocrinology : Rb&E
Zou, Weiwei W; Wang, Binbin B; Wang, Jing J; Zhang, Zhiguo Z; Xu, Xiaofeng X; Chen, Beili B; Ma, Xu X; Cao, Yunxia Y
Publication Date: 2015-06-17
Variant appearance in text: rs35352882
PubMed Link:
26082156
Variant Present in the following documents:
Main text
12958_2015_Article_57.pdf
View BVdb publication page