PPP1R9A c.1395+60014G>A

Variant ID: 7-94600834-G-A

NM_001166160.1(PPP1R9A):c.1395+60014G>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:

Incorporating information from markers in LD with test locus for detecting imprinting and maternal effects.

European Journal Of Human Genetics : Ejhg
Zhang, Fangyuan F; Lin, Shili S
Publication Date: 2020-08

Variant appearance in text: rs854721
PubMed Link: 32080366
Variant Present in the following documents:
  • Main text
View BVdb publication page