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MRVI1 c.226-3117T>C
Variant ID: 11-10658735-A-G
NM_130385.3(
MRVI1
):c.226-3117T>C
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:
STEPS: an efficient prospective likelihood approach to genetic association analyses of secondary traits in extreme phenotype sequencing.
Biostatistics (Oxford, England)
Bi, Wenjian W; Li, Yun Y; Smeltzer, Matthew P MP; Gao, Guimin G; Zhao, Shengli S; Kang, Guolian G
Publication Date: 2020-01-01
Variant appearance in text: rs1035691
PubMed Link:
30007308
Variant Present in the following documents:
Main text
View BVdb publication page