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SNTB1 c.997-22973C>T
Variant ID: 8-121610438-G-A
NM_021021.3(
SNTB1
):c.997-22973C>T
This variant was identified in 4 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Applications of Genomics and Transcriptomics in Precision Medicine for Myopia Control or Prevention.
Biomolecules
Jiang, Liqin L; Goh, Dong Xuan DX; Koh, James Hao Zhong JHZ; Chan, Xavier X; Brennan, Noel A NA; Barathi, Veluchamy Amutha VA; Hoang, Quan V QV
Publication Date: 2023-03-07
Variant appearance in text: rs6469937
PubMed Link:
36979429
Variant Present in the following documents:
Main text
biomolecules-13-00494.pdf
View BVdb publication page
Establishment and characterization of a new mantle cell lymphoma cell line with a NOTCH2 mutation, Arbo.
Ejhaem
Safa, Firas F; Rasmussen, Terri T; Lobelle-Rich, Patricia P; Collier, Stephanie S; Milligan, Nicholas N; Schmeig, John J; Schmid, Janet J; Wiewiorowski, Carol C; Totaro, Denise D; Brown, Theresa C TC; Satyavarapu, Ishwarya I; Badoo, Melody M; Ungerleider, Nathan N; Flemington, Erik K EK; Safah, Hana H; Saba, Nakhle S NS
Publication Date: 2022-11
Variant appearance in text: rs6469937
PubMed Link:
36467812
Variant Present in the following documents:
JHA2-3-1326-s001.xlsx, sheet 1
View BVdb publication page
Insight into the molecular genetics of myopia.
Molecular Vision
Li, Jiali J; Zhang, Qingjiong Q
Publication Date: 2017
Variant appearance in text: rs6469937
PubMed Link:
29386878
Variant Present in the following documents:
Main text
mv-v23-1048.pdf
View BVdb publication page
Association and interaction of myopia with SNP markers rs13382811 and rs6469937 at ZFHX1B and SNTB1 in Han Chinese and European populations.
Molecular Vision
Li, Jiali J; Jiao, Xiaodong X; Zhang, Qingjiong Q; Hejtmancik, J Fielding JF
Publication Date: 2017
Variant appearance in text: rs6469937
PubMed Link:
28848321
Variant Present in the following documents:
Main text
mv-v23-588.pdf
View BVdb publication page