RUNX2 c.423+3201A>G

Variant ID: 6-45393895-A-G

NM_001024630.3(RUNX2):c.423+3201A>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:

A reference haplotype panel for genome-wide imputation of short tandem repeats.

Nature Communications
Saini, Shubham S; Mitra, Ileena I; Mousavi, Nima N; Fotsing, Stephanie Feupe SF; Gymrek, Melissa M
Publication Date: 2018-10-23

Variant appearance in text: rs9472489
PubMed Link: 30353011
Variant Present in the following documents:
  • Main text
  • 41467_2018_Article_6694.pdf
View BVdb publication page