PAFAH1B1 c.33-4399G>A

Variant ID: 17-2564267-G-A

NM_000430.3(PAFAH1B1):c.33-4399G>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:

Association of Autism Spectrum Disorder, Neuroticism, and Subjective Well-Being With Cardiovascular Diseases: A Two-Sample Mendelian Randomization Study.

Frontiers In Cardiovascular Medicine
Sun, Xingang X; Chen, Lu L; Wang, Zhen Z; Lu, Yunlong Y; Chen, Miao M; He, Yuxian Y; Xu, Hongfei H; Zheng, Liangrong L
Publication Date: 2021

Variant appearance in text: rs7218235
PubMed Link: 34179139
Variant Present in the following documents:
  • Main text
  • fcvm-08-676030.pdf
View BVdb publication page