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ATP13A2 c.10+833C>T
Variant ID: 1-17337391-G-A
NM_022089.2(
ATP13A2
):c.10+833C>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:
ATP13A2 (PARK9) polymorphisms influence the neurotoxic effects of manganese.
Neurotoxicology
Rentschler, Gerda G; Covolo, Loredana L; Haddad, Amelia Ahmadi AA; Lucchini, Roberto G RG; Zoni, Silvia S; Broberg, Karin K
Publication Date: 2012-08
Variant appearance in text: rs2076600
PubMed Link:
22285144
Variant Present in the following documents:
Main text
View BVdb publication page