Annotation
Position
chr1 : 197099068
Genotype
G/A,C
Gene
HGVS DNA code
HGVS=ASPM:NM_001206846:exon8:c.2606C>T:p.T869I,ASPM:NM_018136:exon8:c.2606C>T:p.T869I,
HGVS protein code
Author:
GeneTalk
dbSNP Flags:
- Has SubmitterLinkOut (From SNP->SubSNP->Batch.link_out)
- SNP is Clinical (LSDB,OMIM,TPA,Diagnostic)
- SNP is Precious (Clinical,Pubmed Cited)
- Weight=1. (Weight on NCBI reference assembly.)
- Marker is on high density genotyping kit (50K density or greater). The snp may have phenotype associations present in dbGaP.
- Genotypes available. The snp has individual genotype (in SubInd table).
- RS Cluster has none TGP Submission(set VCF OTHERKG).
- HapMap Phase 3 genotyped: filtered, non- redundant. (VCF: PH3)
- Submitted from a locus-specific database.
- Single base polymorphism SNP
- SNP is Clinical (LSDB,OMIM,TPA,Diagnostic)
- SNP is Precious (Clinical,Pubmed Cited)
- Weight=1. (Weight on NCBI reference assembly.)
- Marker is on high density genotyping kit (50K density or greater). The snp may have phenotype associations present in dbGaP.
- Genotypes available. The snp has individual genotype (in SubInd table).
- RS Cluster has none TGP Submission(set VCF OTHERKG).
- HapMap Phase 3 genotyped: filtered, non- redundant. (VCF: PH3)
- Submitted from a locus-specific database.
- Single base polymorphism SNP
Created at March 09, 2013 13:09, Last update March 09, 2013 13:09
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