SPTLC2 c.850+361G>A

Variant ID: 14-78028378-C-T

NM_004863.3(SPTLC2):c.850+361G>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:

Exploiting SNP correlations within random forest for genome-wide association studies.

Plos One
Botta, Vincent V; Louppe, Gilles G; Geurts, Pierre P; Wehenkel, Louis L
Publication Date: 2014

Variant appearance in text: rs4903604
PubMed Link: 24695491
Variant Present in the following documents:
  • Main text
  • pone.0093379.s001.pdf
View BVdb publication page