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MLXIPL c.1671+32T>C
Variant ID: 7-73011163-A-G
NM_032951.2(
MLXIPL
):c.1671+32T>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:
Exome sequencing of 85 Williams-Beuren syndrome cases rules out coding variation as a major contributor to remaining variance in social behavior.
Molecular Genetics & Genomic Medicine
Kopp, Nathan D ND; Parrish, Phoebe C R PCR; Lugo, Michael M; Dougherty, Joseph D JD; Kozel, Beth A BA
Publication Date: 2018-09
Variant appearance in text: rs782188633
PubMed Link:
30008175
Variant Present in the following documents:
MGG3-6-749-s003.xlsx, sheet 1
View BVdb publication page