YWHAG c.87+9810G>T

Variant ID: 7-75978229-C-A

NM_012479.3(YWHAG):c.87+9810G>T

This variant was identified in 2 publications

View GRCh38 version.



Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP

Publications:

Breakdown of multiple sclerosis genetics to identify an integrated disease network and potential variant mechanisms.

Physiological Genomics
Shepard, C Joy CJ; Cline, Sara G SG; Hinds, David D; Jahanbakhsh, Seyedehameneh S; Prokop, Jeremy W JW
Publication Date: 2019-11-01

Variant appearance in text: rs17149161
PubMed Link: 31482761
Variant Present in the following documents:
  • Main text
View BVdb publication page


Genome-wide association study of severity in multiple sclerosis.

Genes And Immunity
,
Publication Date: 2011-12

Variant appearance in text: rs17149161
PubMed Link: 21654844
Variant Present in the following documents:
  • Main text
View BVdb publication page