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PARP14 c.4001-1168G>A
Variant ID: 3-122435750-G-A
NM_017554.2(
PARP14
):c.4001-1168G>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:
Using published data in Mendelian randomization: a blueprint for efficient identification of causal risk factors.
European Journal Of Epidemiology
Burgess, Stephen S; Scott, Robert A RA; Timpson, Nicholas J NJ; Davey Smith, George G; Thompson, Simon G SG; ,
Publication Date: 2015-07
Variant appearance in text: rs2063515
PubMed Link:
25773750
Variant Present in the following documents:
10654_2015_11_MOESM1_ESM.pdf
View BVdb publication page