Annotation Detail
Information
- Associated Genes
- ISG15 NOC2L C1orf159 HES4 PLEKHN1 PERM1 SAMD11 KLHL17 AGRN RNF223 LINC02593 LOC100288175 LOC105378948 LOC107985728 LOC126805576 LOC129929061 LOC129929062 LOC129929063 LOC129929064 LOC129929065 LOC129929066 LOC129929067 LOC129929068 LOC129929069 LOC129929070 LOC129929071 LOC129929072 LOC129929073 LOC129929074 LOC129929075 LOC129929076 LOC129929077 LOC129929078 LOC129929079 LOC129929080 LOC129929081 LOC129929082 LOC129929083 LOC129929084
- Associated Variants
-
GRCh38/hg38 1p36.33(chr1:911300-1084417)x3
GRCh38/hg38 1p36.33(chr1:911300-1084417)x3 - Source Database
- ClinVar
- Description
- GRCh38/hg38 1p36.33(chr1:911300-1084417)x3 AND See cases
- ClinVar Allele ID
- 72083
- Clinical Significance Description
- Uncertain significance
- Clinical Significance Last Update
- 2011-08-12
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000051198
- Observed Origin Sample
- not provided
Drugs