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ZNF782 c.245-2820C>T
Variant ID: 9-99584880-G-A
NM_001001662.1(
ZNF782
):c.245-2820C>T
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:
Genome-wide association scan for stature in Chinese: evidence for ethnic specific loci.
Human Genetics
Lei, Shu-Feng SF; Yang, Tie-Lin TL; Tan, Li-Jun LJ; Chen, Xiang-Ding XD; Guo, Yan Y; Guo, Yan-Fang YF; Zhang, Liang L; Liu, Xiao-Gang XG; Yan, Han H; Pan, Feng F; Zhang, Zhi-Xin ZX; Peng, Yu-Mei YM; Zhou, Qi Q; He, Li-Na LN; Zhu, Xue-Zhen XZ; Cheng, Jing J; Liu, Yao-Zhong YZ; Papasian, Christopher J CJ; Deng, Hong-Wen HW
Publication Date: 2009-02
Variant appearance in text: rs7859940
PubMed Link:
19030899
Variant Present in the following documents:
Main text
View BVdb publication page
Genome-wide SNP typing reveals signatures of population history.
Genomics
Hughes, Austin L AL; Welch, Robert R; Puri, Vinita V; Matthews, Casey C; Haque, Kashif K; Chanock, Stephen J SJ; Yeager, Meredith M
Publication Date: 2008-07
Variant appearance in text: rs7859940
PubMed Link:
18485661
Variant Present in the following documents:
Main text
View BVdb publication page