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FGG c.667-49T>G
Variant ID: 4-155529851-A-C
NM_021870.2(
FGG
):c.667-49T>G
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:
Gene variants as risk factors for gastroschisis.
American Journal Of Medical Genetics. Part A
Padula, Amy M AM; Yang, Wei W; Schultz, Kathleen K; Tom, Lauren L; Lin, Bin B; Carmichael, Suzan L SL; Lammer, Edward J EJ; Shaw, Gary M GM
Publication Date: 2016-11
Variant appearance in text: rs6064
PubMed Link:
27616475
Variant Present in the following documents:
Main text
AJMG-170-2788.pdf
View BVdb publication page