SEH1L c.621-1545A>C

Variant ID: 18-12977206-A-C

NM_001013437.1(SEH1L):c.621-1545A>C

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:

Ranking causal variants and associated regions in genome-wide association studies by the support vector machine and random forest.

Nucleic Acids Research
Roshan, Usman U; Chikkagoudar, Satish S; Wei, Zhi Z; Wang, Kai K; Hakonarson, Hakon H
Publication Date: 2011-05

Variant appearance in text: rs8088313
PubMed Link: 21317188
Variant Present in the following documents:
  • supp_gkr064_supplementarygkr064.pdf
View BVdb publication page