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MPHOSPH9 c.1087+1760A>T
Variant ID: 12-123697531-T-A
NM_022782.3(
MPHOSPH9
):c.1087+1760A>T
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:
Exploring Potential Causal Genes for Uterine Leiomyomas: A Summary Data-Based Mendelian Randomization and FUMA Analysis.
Frontiers In Genetics
Dai, Yuxin Y; Liu, Xudong X; Zhu, Yining Y; Mao, Su S; Yang, Jingyun J; Zhu, Lan L
Publication Date: 2022
Variant appearance in text: rs10772996
PubMed Link:
35903355
Variant Present in the following documents:
Main text
fgene-13-890007.pdf
View BVdb publication page