Bibliome.ai browser hg19
Search
About
Stats
FAQ
PAX2 c.410+13822G>A
Variant ID: 10-102524470-G-A
NM_000278.3(
PAX2
):c.410+13822G>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:
Evaluation of High Resolution Melting analysis as an alternate tool to screen for risk alleles associated with small kidneys in Indian newborns.
Bmc Nephrology
Raghavendra, Ashwini A; Siji, Annes A; Sridhar, T S TS; Phadke, Kishore K; Vasudevan, Anil A
Publication Date: 2011-10-28
Variant appearance in text: rs11190688
PubMed Link:
22035350
Variant Present in the following documents:
Main text
1471-2369-12-60.pdf
View BVdb publication page