HAPLN1 c.-26-16781A>G

Variant ID: 5-82986149-T-C

NM_001884.3(HAPLN1):c.-26-16781A>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:

Functional screening of Alzheimer pathology genome-wide association signals in Drosophila.

American Journal Of Human Genetics
Shulman, Joshua M JM; Chipendo, Portia P; Chibnik, Lori B LB; Aubin, Cristin C; Tran, Dong D; Keenan, Brendan T BT; Kramer, Patricia L PL; Schneider, Julie A JA; Bennett, David A DA; Feany, Mel B MB; De Jager, Philip L PL
Publication Date: 2011-02-11

Variant appearance in text: rs16898
PubMed Link: 21295279
Variant Present in the following documents:
  • Main text
View BVdb publication page