Annotation
Position
chr11 : 111965693
Genotype
G/T
Gene
HGVS DNA code
NM_003002.3:c.479G>T
HGVS protein code
Author:
Text:
The term `not provided` is registered in MedGen to support identification of submissions to ClinVar for which no condition was named when assessing the variant. `not provided` differs from `not specified`, which is used when a variant is asserted to be benign, likely benign, or of uncertain significance for conditions that have not been specified.
Created at August 08, 2015 15:04, Last update August 08, 2015 15:04
Voting

Clinical significance
Pathogenic
Votes
Stars | Clinical significance |
---|---|
5 | 3 votes |
4 | 0 votes |
3 | 0 votes |
2 | 0 votes |
1 | 0 votes |
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