CBLC c.1363-327G>A

Variant ID: 19-45303311-G-A

NM_012116.3(CBLC):c.1363-327G>A

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:

Prospects of Fine-Mapping Trait-Associated Genomic Regions by Using Summary Statistics from Genome-wide Association Studies.

American Journal Of Human Genetics
Benner, Christian C; Havulinna, Aki S AS; Järvelin, Marjo-Riitta MR; Salomaa, Veikko V; Ripatti, Samuli S; Pirinen, Matti M
Publication Date: 2017-10-05

Variant appearance in text: rs10418198
PubMed Link: 28942963
Variant Present in the following documents:
  • Main text
View BVdb publication page