HBS1L c.1306-164A>C

Variant ID: 6-135307485-T-G

NM_006620.3(HBS1L):c.1306-164A>C

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:

Genetic modifiers of Hb E/beta0 thalassemia identified by a two-stage genome-wide association study.

Bmc Medical Genetics
Sherva, Richard R; Sripichai, Orapan O; Abel, Kenneth K; Ma, Qianli Q; Whitacre, Johanna J; Angkachatchai, Vach V; Makarasara, Wattanan W; Winichagoon, Pranee P; Svasti, Saovaros S; Fucharoen, Suthat S; Braun, Andreas A; Farrer, Lindsay A LA
Publication Date: 2010-03-30

Variant appearance in text: rs4376364
PubMed Link: 20353593
Variant Present in the following documents:
  • Main text
  • 1471-2350-11-51.pdf
View BVdb publication page