Annotation
Position
chr15 : 73615051
Genotype
C/A
Gene
HGVS DNA code
NM_005477.2:c.3383G>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 15:06, Last update August 08, 2015 15:06
Voting

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