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RERE c.522+15908A>C
Variant ID: 1-8658712-T-G
NM_001042681.1(
RERE
):c.522+15908A>C
This variant was identified in 3 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Multiomics dissection of molecular regulatory mechanisms underlying autoimmune-associated noncoding SNPs.
Jci Insight
Chen, Xiao-Feng XF; Guo, Ming-Rui MR; Duan, Yuan-Yuan YY; Jiang, Feng F; Wu, Hao H; Dong, Shan-Shan SS; Zhou, Xiao-Rong XR; Thynn, Hlaing Nwe HN; Liu, Cong-Cong CC; Zhang, Lin L; Guo, Yan Y; Yang, Tie-Lin TL
Publication Date: 2020-09-03
Variant appearance in text: rs1318218
PubMed Link:
32879140
Variant Present in the following documents:
jciinsight-5-136477-s105.xlsx, sheet 5
View BVdb publication page
Genome-wide association and HLA region fine-mapping studies identify susceptibility loci for multiple common infections.
Nature Communications
Tian, Chao C; Hromatka, Bethann S BS; Kiefer, Amy K AK; Eriksson, Nicholas N; Noble, Suzanne M SM; Tung, Joyce Y JY; Hinds, David A DA
Publication Date: 2017-09-19
Variant appearance in text: rs1318218
PubMed Link:
28928442
Variant Present in the following documents:
41467_2017_257_MOESM1_ESM.pdf
View BVdb publication page
Detection and interpretation of shared genetic influences on 42 human traits.
Nature Genetics
Pickrell, Joseph K JK; Berisa, Tomaz T; Liu, Jimmy Z JZ; Ségurel, Laure L; Tung, Joyce Y JY; Hinds, David A DA
Publication Date: 2016-07
Variant appearance in text: rs1318218
PubMed Link:
27182965
Variant Present in the following documents:
NIHMS780506-supplement-16.pdf
View BVdb publication page