Bibliome.ai browser hg19
Search
About
Stats
FAQ
ESR1 c.761-24885A>G
Variant ID: 6-152240423-A-G
NM_000125.3(
ESR1
):c.761-24885A>G
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:
Bivariate Genome-Wide Association Study Implicates ATP6V1G1 as a Novel Pleiotropic Locus Underlying Osteoporosis and Age at Menarche.
The Journal Of Clinical Endocrinology And Metabolism
Tan, Li-Jun LJ; Wang, Zhuo-Er ZE; Wu, Ke-Hao KH; Chen, Xiang-Ding XD; Zhu, Hu H; Lu, Shan S; Tian, Qing Q; Liu, Xiao-Gang XG; Papasian, Christopher J CJ; Deng, Hong-Wen HW
Publication Date: 2015-11
Variant appearance in text: rs4458702
PubMed Link:
26312577
Variant Present in the following documents:
Main text
View BVdb publication page
Genetic factors influencing bone mineral content in a black South African population.
Journal Of Bone And Mineral Metabolism
May, Andrew A; Pettifor, John M JM; Norris, Shane A SA; Ramsay, Michèle M; Lombard, Zané Z
Publication Date: 2013-11
Variant appearance in text: rs4458702
PubMed Link:
23475190
Variant Present in the following documents:
Main text
774_2013_Article_431.pdf
View BVdb publication page