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SLC9A9 c.378+5099C>T
Variant ID: 3-143545762-G-A
NM_173653.3(
SLC9A9
):c.378+5099C>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:
Construction of gene clusters resembling genetic causal mechanisms for common complex disease with an application to young-onset hypertension.
Bmc Genomics
Lynn, Ke-Shiuan KS; Lu, Chen-Hua CH; Yang, Han-Ying HY; Hsu, Wen-Lian WL; Pan, Wen-Harn WH
Publication Date: 2013-07-23
Variant appearance in text: rs16854417
PubMed Link:
23879630
Variant Present in the following documents:
Main text
1471-2164-14-497.pdf
View BVdb publication page