JAK2 c.3060-13473C>T

Variant ID: 9-5109531-C-T

NM_004972.3(JAK2):c.3060-13473C>T

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:

Haplotype kernel association test as a powerful method to identify chromosomal regions harboring uncommon causal variants.

Genetic Epidemiology
Lin, Wan-Yu WY; Yi, Nengjun N; Lou, Xiang-Yang XY; Zhi, Degui D; Zhang, Kui K; Gao, Guimin G; Tiwari, Hemant K HK; Liu, Nianjun N
Publication Date: 2013-09

Variant appearance in text: rs10491652
PubMed Link: 23740760
Variant Present in the following documents:
  • Main text
View BVdb publication page