"Illumina Laboratory Services, Illumina"[submitter] AND "LOC129999670" - ClinVar - NCBI

Warning: The NCBI web site requires JavaScript to function. more...

Display options Sort by Location Download

Format

Tabular
Tabular (text)
UI List

Sort by

Location
Relevance
Gene
Variation

Choose Destination

File

Search results

Items: 3

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 359365	NM_016203.3(PRKAG2):c.-560C>T	LOC129999670, PRKAG2 +1 more	Single nucleotide variant	Familial Hypertrophic Cardiomyopathy with Wolff-Parkinson-White Syndrome +2 more	GBenign/Likely benign
Select item 359366	NM_016203.3(PRKAG2):c.-575C>T	LOC129999670, PRKAG2 +1 more	Single nucleotide variant	Familial Hypertrophic Cardiomyopathy with Wolff-Parkinson-White Syndrome +2 more	GUncertain significance
Select item 359367	NM_016203.3(PRKAG2):c.-580C>T	LOC129999670, PRKAG2 +1 more	Single nucleotide variant	Familial Hypertrophic Cardiomyopathy with Wolff-Parkinson-White Syndrome +2 more	GUncertain significance

Display options Sort by Location Download

Format

Tabular
Tabular (text)
UI List

Sort by

Location
Relevance
Gene
Variation

Choose Destination

File