Bibliome.ai browser hg19
Search
About
Stats
FAQ
VDR c.-84+946T>C
Variant ID: 12-48297792-A-G
NM_000376.3(
VDR
):c.-84+946T>C
This variant was identified in 2 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Whole genome sequencing identifies high-impact variants in well-known pharmacogenomic genes.
The Pharmacogenomics Journal
Choi, Jihoon J; Tantisira, Kelan G KG; Duan, Qing Ling QL
Publication Date: 2019-04
Variant appearance in text: rs7979360
PubMed Link:
30214008
Variant Present in the following documents:
NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page
Maternal vitamin D receptor genetic variation contributes to infant birthweight among black mothers.
American Journal Of Medical Genetics. Part A
Swamy, Geeta K GK; Garrett, Melanie E ME; Miranda, Marie Lynn ML; Ashley-Koch, Allison E AE
Publication Date: 2011-06
Variant appearance in text: rs7979360
PubMed Link:
21548019
Variant Present in the following documents:
Main text
View BVdb publication page