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LDLRAD2 c.511+7T>G
Variant ID: 1-22141323-T-G
NM_001013693.2(
LDLRAD2
):c.511+7T>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:
Feeding difficulty is the dominant feature in 12 Chinese newborns with CHD7 pathogenic variants.
Bmc Medical Genetics
Chen, Xiang X; Yan, Kai K; Gao, Yanyan Y; Wang, Huijun H; Chen, Guoqiang G; Wu, Bingbing B; Qin, Qian Q; Yang, Lin L; Zhou, Wenhao W
Publication Date: 2019-05-30
Variant appearance in text: LDLRAD2: 511+7T>G
PubMed Link:
31146700
Variant Present in the following documents:
12881_2019_813_MOESM1_ESM.xls, sheet 1
View BVdb publication page