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DTD1 c.478-5883T>G
Variant ID: 20-18718861-T-G
NM_080820.4(
DTD1
):c.478-5883T>G
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:
Genome-wide association study of severity in multiple sclerosis.
Genes And Immunity
,
Publication Date: 2011-12
Variant appearance in text: rs6075409
PubMed Link:
21654844
Variant Present in the following documents:
Main text
View BVdb publication page