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PPARG c.1180+7837A>G
Variant ID: 3-12466490-A-G
NM_138711.6(
PPARG
):c.1180+7837A>G
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:
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: rs1177809
PubMed Link:
26312577
Variant Present in the following documents:
Main text
View BVdb publication page